The syndrome of 17,20 lyase deficiency (Q24614420)

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English	The syndrome of 17,20 lyase deficiency	scientific article

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instance of

scholarly article

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title

The syndrome of 17,20 lyase deficiency (English)

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author name string

Walter L Miller

series ordinal

1

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language of work or name

English

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publication date

January 2012

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published in

The Journal of Clinical Endocrinology and Metabolism

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volume

97

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issue

1

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page(s)

59-67

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cites work

Why boys will be boys: two pathways of fetal testicular androgen biosynthesis are needed for male sexual differentiation

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7 April 2017

The Molecular Biology, Biochemistry, and Physiology of Human Steroidogenesis and Its Disorders

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7 April 2017

Between a chicken and a grape: estimating the number of human genes

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7 April 2017

Genetic Control of Biochemical Reactions in Neurospora

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7 April 2017

Diversity and function of mutations in p450 oxidoreductase in patients with Antley-Bixler syndrome and disordered steroidogenesis

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PubMed Central

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7 April 2017

ON THE COLINEARITY OF GENE STRUCTURE AND PROTEIN STRUCTURE

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PubMed Central

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7 April 2017

The genetic and functional basis of isolated 17,20-lyase deficiency

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

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7 April 2017

Three-dimensional structure of NADPH-cytochrome P450 reductase: prototype for FMN- and FAD-containing enzymes

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PubMed Central

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7 April 2017

Expression cloning and characterization of oxidative 17beta- and 3alpha-hydroxysteroid dehydrogenases from rat and human prostate

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

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7 April 2017

Cloning and sequence of the human gene for P450c17 (steroid 17 alpha-hydroxylase/17,20 lyase): similarity with the gene for P450c21

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

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7 April 2017

Conformational Changes of NADPH-Cytochrome P450 Oxidoreductase Are Essential for Catalysis and Cofactor Binding

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

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7 April 2017

NADPH-cytochrome P450 oxidoreductase. Structural basis for hydride and electron transfer

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

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7 April 2017

Regulation of 17,20 lyase activity by cytochrome b5 and by serine phosphorylation of P450c17

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

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7 April 2017

Protein phosphatase 2A and phosphoprotein SET regulate androgen production by P450c17

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

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7 April 2017

Expression and characterization of recombinant type 2 3 alpha-hydroxysteroid dehydrogenase (HSD) from human prostate: demonstration of bifunctional 3 alpha/17 beta-HSD activity and cellular distribution

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

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7 April 2017

Role of steroidogenic acute regulatory protein in adrenal and gonadal steroidogenesis

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

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7 April 2017

Serine phosphorylation of human P450c17 increases 17,20-lyase activity: implications for adrenarche and the polycystic ovary syndrome

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stated in

PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

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7 April 2017

Adrenal changes associated with adrenarche

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

retrieved

27 September 2017

Androgen synthesis in adrenarche

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

retrieved

27 September 2017

Homozygous mutation G539R in the gene for P450 oxidoreductase in a family previously diagnosed as having 17,20-lyase deficiency.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

retrieved

27 September 2017

Pathways leading to phosphorylation of p450c17 and to the posttranslational regulation of androgen biosynthesis

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

retrieved

27 September 2017

Multiple steps determine the overall rate of the reduction of 5alpha-dihydrotestosterone catalyzed by human type 3 3alpha-hydroxysteroid dehydrogenase: implications for the elimination of androgens

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

retrieved

27 September 2017

Human cytochrome b5 requires residues E48 and E49 to stimulate the 17,20-lyase activity of cytochrome P450c17.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

retrieved

27 September 2017

Isolated 17,20-lyase (desmolase) deficiency in a 46,XX female presenting with delayed puberty

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stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

retrieved

27 September 2017

Regulation of cytochrome b5 gene transcription by Sp3, GATA-6, and steroidogenic factor 1 in human adrenal NCI-H295A cells

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stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

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27 September 2017

Minireview: regulation of steroidogenesis by electron transfer

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

retrieved

27 September 2017

The backdoor pathway to dihydrotestosterone

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stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

retrieved

27 September 2017

Deficiency of 17,20-lyase causing giant ovarian cysts in a girl and a female phenotype in her 46,XY sister: case report

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stated in

PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

retrieved

27 September 2017

CYP17 Mutation E305G Causes Isolated 17,20-Lyase Deficiency by Selectively Altering Substrate Binding

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

retrieved

27 September 2017

The adrenogenital syndrome with deficiency of 3 beta-hydroxysteroid dehydrogenase

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

retrieved

27 September 2017

The syndrome of male pseudohermaphrodism in congenital adrenocortical hyperplasia without overproduction of androgens (adrenal male pseudohermaphrodism)

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

retrieved

27 September 2017

Human type 3 3alpha-hydroxysteroid dehydrogenase (aldo-keto reductase 1C2) and androgen metabolism in prostate cells.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

retrieved

27 September 2017

Molecular modeling of human P450c17 (17alpha-hydroxylase/17,20-lyase): insights into reaction mechanisms and effects of mutations.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

retrieved

27 September 2017

Cytochrome b5 augments the 17,20-lyase activity of human P450c17 without direct electron transfer

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stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

retrieved

27 September 2017

Molecular cloning of human type 3 3 alpha-hydroxysteroid dehydrogenase that differs from 20 alpha-hydroxysteroid dehydrogenase by seven amino acids

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

retrieved

27 September 2017

17-hydroxylation deficiency in man

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stated in

PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

retrieved

27 September 2017

Congenital methemoglobinemia with a deficiency of cytochrome b5.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

retrieved

27 September 2017

Expression of bovine 17 alpha-hydroxylase cytochrome P-450 cDNA in nonsteroidogenic (COS 1) cells

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

retrieved

27 September 2017

Cytochrome P450c17 (steroid 17 alpha-hydroxylase/17,20 lyase): cloning of human adrenal and testis cDNAs indicates the same gene is expressed in both tissues

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

retrieved

27 September 2017

Male Pseudohermaphroditism Consistent with 17,20-Desmolase Deficiency

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

retrieved

27 September 2017

Domain motion in cytochrome P450 reductase: conformational equilibria revealed by NMR and small-angle x-ray scattering.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

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30 May 2018

The pathophysiology and genetics of congenital lipoid adrenal hyperplasia.

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

retrieved

30 May 2018

Steroid 17 alpha-hydroxylase and 17,20-lyase activities of P450c17: contributions of serine106 and P450 reductase

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

retrieved

30 May 2018

Male pseudohermaphroditism due to 17,20-desmolase deficiency

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

retrieved

30 May 2018

Microsomal cytochrome P-450 from neonatal pig testis: two enzymatic activities (17 alpha-hydroxylase and c17,20-lyase) associated with one protein

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

retrieved

30 May 2018

Missense mutation serine106—-proline causes 17 alpha-hydroxylase deficiency

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

retrieved

30 May 2018

Molecular basis of apparent isolated 17,20-lyase deficiency: compound heterozygous mutations in the C-terminal region (Arg(496)----Cys, Gln(461)----Stop) actually cause combined 17 alpha-hydroxylase/17,20-lyase deficiency

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

retrieved

30 May 2018

The structure of ferrocytochrome b5 at 2.8 A resolution

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

retrieved

30 May 2018

Isolated 17,20-lyase deficiency due to the cytochrome b5 mutation W27X.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

retrieved

28 November 2018

Modeling of human P450 oxidoreductase structure by in silico mutagenesis and MD simulation

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

retrieved

28 November 2018

Metabolic evidence for impaired 17alpha-hydroxylase activity in a kindred bearing the E305G mutation for isolate 17,20-lyase activity

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

retrieved

28 November 2018

The 17, 20-lyase activity of cytochrome p450c17 from human fetal testis favors the delta5 steroidogenic pathway

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

retrieved

28 November 2018

5alpha-androstane-3alpha,17beta-diol is formed in tammar wallaby pouch young testes by a pathway involving 5alpha-pregnane-3alpha,17alpha-diol-20-one as a key intermediate

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

retrieved

28 November 2018

Differential inhibition of 17alpha-hydroxylase and 17,20-lyase activities by three novel missense CYP17 mutations identified in patients with P450c17 deficiency

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

retrieved

28 November 2018

Pitfalls in characterizing P450c17 mutations associated with isolated 17,20-lyase deficiency

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

retrieved

28 November 2018

Lysine mutagenesis identifies cationic charges of human CYP17 that interact with cytochrome b5 to promote male sex-hormone biosynthesis

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

retrieved

28 November 2018

P450c17 mutations R347H and R358Q selectively disrupt 17,20-lyase activity by disrupting interactions with P450 oxidoreductase and cytochrome b5.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251937

retrieved

28 November 2018

Microsomal cytochrome P-450 from neonatal pig testis. Purification and properties of A C21 steroid side-chain cleavage system (17 alpha-hydroxylase-C17,20 lyase)

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/22072737

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypergonadotrophic hypogonadism in an XX female subject due to 17,20 steroid desmolase deficiency

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/22072737

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Steroid 17,20-desmolase deficiency: a new cause of male pseudohermaphroditism

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/22072737

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Testicular microsomal cytochrome P-450 for C21 steroid side chain cleavage. Spectral and binding studies

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/22072737

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heterogeneity of cytochrome P-450 in rat testis microsomes

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/22072737

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Urine steroid hormone profile analysis in cytochrome P450 oxidoreductase deficiency: implication for the backdoor pathway to dihydrotestosterone

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/22072737

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bovine adrenocortical microsomal hemeproteins P-45017 alpha and P-450C-21. Isolation, partial characterization, and comparison to P-450SCC

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/22072737

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

PHOTOCHEMICAL ACTION SPECTRUM OF THE TERMINAL OXIDASE OF MIXED FUNCTION OXIDASE SYSTEMS

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/22072737

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A splicing mutation in the cytochrome b5 gene from a patient with congenital methemoglobinemia and pseudohermaphrodism

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/22072737

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The hormonal control of sexual development

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/22072737

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Role of electron transport in the regulation of the lyase activity of C21 side-chain cleavage P-450 from porcine adrenal and testicular microsomes

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/22072737

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A single amino acid substitution in the putative redox partner-binding site of P450c17 as cause of isolated 17,20-lyase deficiency

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/22072737

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Conversion from pure 17,20-desmolase- to combined 17,20-desmolase/17 alpha-hydroxylase deficiency with age

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/22072737

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

17,20-desmolase deficiency in a female newborn, paradoxically virilized in utero

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/22072737

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Plasma and urinary corticosteroids in the hypertensive form of congenital adrenal hyperplasia

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/22072737

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial Male Pseudohermaphroditism due to 17–20- Desmolase Deficiency. I.In VivoEndocrine Studies*

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/22072737

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two Types of Male Pseudohermaphroditism due to 17,20-Desmolase Deficiency*

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/22072737

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

C21 steroid side chain cleavage enzyme from porcine adrenal microsomes. Purification and characterization of the 17 alpha-hydroxylase/C17,20-lyase cytochrome P-450

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/22072737

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Testicular function in prepubertal male pseudohermaphroditism

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/22072737

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1210/JC.2011-2161

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PMC publication ID

3251937

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PubMed publication ID

22072737

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