Gene conversion-like events cause steroid 21-hydroxylase deficiency in congenital adrenal hyperplasia (Q34366737)

1 August 2017

title

Gene conversion-like events cause steroid 21-hydroxylase deficiency in congenital adrenal hyperplasia (English)

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1 August 2017

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F Harada

1

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1 August 2017

A Kimura

2

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1 August 2017

T Iwanaga

3

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1 August 2017

K Shimozawa

4

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1 August 2017

J Yata

5

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1 August 2017

T Sasazuki

6

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1 August 2017

language of work or name

English

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publication date

1 November 1987

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Proceedings of the National Academy of Sciences of the United States of America

1 August 2017

published in

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1 August 2017

volume

84

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1 August 2017

issue

22

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1 August 2017

page(s)

8091-8094

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Intrachromosomal gene conversion and the maintenance of sequence homogeneity among repeated genes.

1 August 2017

cites work

1 reference

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Unusual evolutionary conservation and frequent DNA segment exchange in class I genes of the major histocompatibility complex

6 July 2018

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The structural basis of the multiple forms of human complement component C4.

6 July 2018

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HLA-linked congenital adrenal hyperplasia results from a defective gene encoding a cytochrome P-450 specific for steroid 21-hydroxylation

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=299484

Mapping of steroid 21-hydroxylase genes adjacent to complement component C4 genes in HLA, the major histocompatibility complex in man.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=299484

Frequent deletion and duplication of the steroid 21-hydroxylase genes

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=299484

Structure of human steroid 21-hydroxylase genes

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=299484

Complete nucleotide sequence of two steroid 21-hydroxylase genes tandemly arranged in human chromosome: a pseudogene and a genuine gene

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=299484

Gene conversion in a cytochrome P-450 gene family

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=299484

Deletion of complement C4 and steroid 21-hydroxylase genes in the HLA class III region

6 July 2018

1 reference

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Two genes encoding steroid 21-hydroxylase are located near the genes encoding the fourth component of complement in man

6 July 2018

1 reference

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Detection of specific sequences among DNA fragments separated by gel electrophoresis

6 July 2018

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DNA sequencing with chain-terminating inhibitors

6 July 2018

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Microdroplet testing for HLA-A, -B, -C, and -D antigens. The Phillip Levine Award Lecture

6 July 2018

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Statement on the nomenclature of human C4 allotypes.

6 July 2018

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Two steroid 21-hydroxylase genes are located in the murine S region

27 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/3500473

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Neonatal screening for congenital adrenal hyperplasia in Japan

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/3500473

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Gene conversion in salt-losing congenital adrenal hyperplasia with absent complement C4B protein

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/3500473

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1073/PNAS.84.22.8091

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1 August 2017

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1 August 2017

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