Mutation of HSD3B2 Gene and Fate of Dehydroepiandrosterone-Reference-Cited by-同舟云学术

Mutation of HSD3B2 Gene and Fate of Dehydroepiandrosterone

Published:2018 Issue: Volume: Page:75-123
ISSN:0083-6729
Container-title:Dehydroepiandrosterone
language:
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Author:

Baquedano Maria Sonia,Guercio Gabriela,Costanzo Mariana,Marino Roxana,Rivarola Marco A.,Belgorosky Alicia

Publisher

Elsevier

Reference119 articles.

1. A novel A10E homozygous mutation in the HSD3B2 gene causing severe salt-wasting 3beta-hydroxysteroid dehydrogenase deficiency in 46,XX and 46,XY French-Canadians: Evaluation of gonadal function after puberty;Alos;The Journal of Clinical Endocrinology and Metabolism,2000

2. The adrenal cortex and sexual differentiation during early human development;Asby;Reviews in Endocrine & Metabolic Disorders,2009

3. The backdoor pathway to dihydrotestosterone;Auchus;Trends in Endocrinology and Metabolism: TEM,2004

4. The physiology and biochemistry of adrenarche;Auchus;Endocrine Development,2011

5. 46,XX DSD: The masculinised female;Auchus;Best Practice & Research Clinical Endocrinology & Metabolism,2010

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