Gene Conversions and Rearrangements Cause Discordance Between Inheritance of Forms of 21-Hydroxylase Deficiency and HLA Types*-Reference-Cited by-同舟云学术

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Gene Conversions and Rearrangements Cause Discordance Between Inheritance of Forms of 21-Hydroxylase Deficiency and HLA Types*

Published:1989-03 Issue:3 Volume:68 Page:592-599
ISSN:0021-972X
Container-title:The Journal of Clinical Endocrinology & Metabolism
language:en
Short-container-title:The Journal of Clinical Endocrinology & Metabolism

Author:

MOREL YVES,DAVID MICHEL,FOREST MAGUELONE G.,BETUEL HERVE,HAUPTMAN GEORGES,ANDRE JEAN,BERTRAND JEAN,MILLER WALTER L.

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Link

http://academic.oup.com/jcem/article-pdf/68/3/592/10500678/jcem0592.pdf

Cited by 42 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Assessment of the most common CYP21A2 point mutations in a cohort of congenital adrenal hyperplasia patients from Egypt;Journal of Pediatric Endocrinology and Metabolism;2020-07-01

2. Defects of Adrenal Steroidogenesis;Endocrinology: Adult and Pediatric;2016

3. Abiraterone Acetate to Lower Androgens in Women With Classic 21-Hydroxylase Deficiency;The Journal of Clinical Endocrinology & Metabolism;2014-08-01

4. Impact of Genome Complexity of the CYP21A2 Gene on Adrenal Steroidogenesis;Journal of Experimental & Clinical Medicine;2012-12

5. The Molecular Biology, Biochemistry, and Physiology of Human Steroidogenesis and Its Disorders;Endocrine Reviews;2011-02-01

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