17-α-Hydroxylase Deficiency Due to P.R362C Mutation in two Sisters From India-Reference-Cited by-同舟云学术

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17-α-Hydroxylase Deficiency Due to P.R362C Mutation in two Sisters From India

Published:2017 Issue:4 Volume:3 Page:322-325
ISSN:2376-0605
Container-title:AACE Clinical Case Reports
language:en
Short-container-title:AACE Clinical Case Reports

Author:

Roy Ajitesh,Bhattacharjee Rana,Goswami Soumik,Chakraborty Partha P.,Chitra S.,Thukral Anubhab,Sadhukhan Susanta,Bankura Biswabandhu,Das Madhusudan,Biswas Kousik,Chowdhury Subhankar

Publisher

Elsevier BV

Reference7 articles.

1. The adrenal cortex;Stewart,2016

2. Localization of the human CYP17 gene (cytochrome P45017α) to 10q24.3 by fluorescence in situ hybridization and simultaneous chromosome banding;Fan;Genomics,1992

3. Novel CYP17A1 mutation in a Japanese patient with combined 17alpha-hydroxylase/17,20-lyase deficiency;Katsumata;Metabolism,2010

4. 17 Alpha-hydroxylase deficiency: 1963–1966;Biglieri;J Clin Endocrinol Metab,1997

5. Two types of male pseudohermaphroditism due to 17,20-desmolase deficiency;Zachmann;J Clin Endocrinol Metab,1982

Cited by 2 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. Clinical, biochemical and genetic characteristics of children with congenital adrenal hyperplasia due to 17α-hydroxylase deficiency;Journal of Pediatric Endocrinology and Metabolism;2020-07-11

2. A challenging case of primary amenorrhoea;BMJ Case Reports;2018-07-11

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