Genetic heterogeneity and mitochondrial DNA heteroplasmy in Leber's hereditary optic neuropathy. (Q33593412)

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English	Genetic heterogeneity and mitochondrial DNA heteroplasmy in Leber's hereditary optic neuropathy.	scientific article

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scholarly article

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Europe PubMed Central

PMC publication ID

1015752

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2575667%20AND%20SRC:MED&resulttype=core&format=json

retrieved

1 October 2019

title

Genetic heterogeneity and mitochondrial DNA heteroplasmy in Leber's hereditary optic neuropathy (English)

1 reference

stated in

Europe PubMed Central

PMC publication ID

1015752

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2575667%20AND%20SRC:MED&resulttype=core&format=json

retrieved

1 October 2019

main subject

mitochondrial DNA

0 references

heteroplasmy

1 reference

based on heuristic

inferred from title

author

Ian Holt

series ordinal

1

1 reference

stated in

Europe PubMed Central

PMC publication ID

1015752

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2575667%20AND%20SRC:MED&resulttype=core&format=json

retrieved

1 October 2019

author name string

D H Miller

series ordinal

2

1 reference

stated in

Europe PubMed Central

PMC publication ID

1015752

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2575667%20AND%20SRC:MED&resulttype=core&format=json

retrieved

1 October 2019

A E Harding

series ordinal

3

1 reference

stated in

Europe PubMed Central

PMC publication ID

1015752

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2575667%20AND%20SRC:MED&resulttype=core&format=json

retrieved

1 October 2019

language of work or name

English

0 references

publication date

1 December 1989

1 reference

stated in

Europe PubMed Central

PMC publication ID

1015752

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2575667%20AND%20SRC:MED&resulttype=core&format=json

retrieved

1 October 2019

published in

Journal of Medical Genetics

1 reference

stated in

Europe PubMed Central

PMC publication ID

1015752

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2575667%20AND%20SRC:MED&resulttype=core&format=json

retrieved

1 October 2019

volume

26

1 reference

stated in

Europe PubMed Central

PMC publication ID

1015752

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2575667%20AND%20SRC:MED&resulttype=core&format=json

retrieved

1 October 2019

issue

12

1 reference

stated in

Europe PubMed Central

PMC publication ID

1015752

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2575667%20AND%20SRC:MED&resulttype=core&format=json

retrieved

1 October 2019

page(s)

739-743

1 reference

stated in

Europe PubMed Central

PMC publication ID

1015752

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2575667%20AND%20SRC:MED&resulttype=core&format=json

retrieved

1 October 2019

cites work

Sequence and organization of the human mitochondrial genome

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=1015752

retrieved

21 June 2018

A technique for radiolabeling DNA restriction endonuclease fragments to high specific 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=1015752

retrieved

21 June 2018

Maternal inheritance of human mitochondrial DNA

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=1015752

retrieved

21 June 2018

Leber's optic atrophy, a possible example of maternal inheritance.

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=1015752

retrieved

21 June 2018

Six unidentified reading frames of human mitochondrial DNA encode components of the respiratory-chain NADH 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=1015752

retrieved

21 June 2018

Deletions of mitochondrial DNA in Kearns-Sayre syndrome

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=1015752

retrieved

21 June 2018

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

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=1015752

retrieved

21 June 2018

Mitochondrial DNA-like sequences in the human nuclear genome. Characterization and implications in the evolution of mitochondrial DNA.

1 reference

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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=1015752

retrieved

21 June 2018

Restriction endonuclease analysis of leukocyte mitochondrial DNA in Leber's optic atrophy

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=1015752

retrieved

21 June 2018

Duplications of mitochondrial DNA in mitochondrial myopathy

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=1015752

retrieved

21 June 2018

A defect in mitochondrial electron-transport activity (NADH-coenzyme Q oxidoreductase) in Leber's hereditary optic neuropathy.

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=1015752

retrieved

21 June 2018

Conservation of genes coding for proteins synthesized in human mitochondria

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=1015752

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21 June 2018

Leber's optic neuropathy: a clinical and visual evoked potential study of affected and asymptomatic members of a six generation family

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2575667

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ophthalmoscopic findings in Leber's hereditary optic neuropathy. II. The fundus findings in the affected family members

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2575667

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Leber's hereditary optic neuroretinopathy, a maternally inherited disease. A genealogic study in four pedigrees

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2575667

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2575667

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identical mitochondrial DNA deletion in blood and muscle

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2575667

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1136/JMG.26.12.739

1 reference

stated in

Europe PubMed Central

PMC publication ID

1015752

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2575667%20AND%20SRC:MED&resulttype=core&format=json

retrieved

1 October 2019

PMC publication ID

1015752

1 reference

stated in

Europe PubMed Central

PMC publication ID

1015752

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2575667%20AND%20SRC:MED&resulttype=core&format=json

retrieved

1 October 2019

PubMed publication ID

2575667

1 reference

stated in

Europe PubMed Central

PMC publication ID

1015752

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2575667%20AND%20SRC:MED&resulttype=core&format=json

retrieved

1 October 2019

 

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