Mutation Analysis of the CYP21A2 Gene in the Iranian Population

Background: Defects in the CYP21A2 gene cause steroid 21-hydroxylase deficiency, which is the most frequent cause of congenital adrenal hyperplasia. Forty four affected families were investigated to identify the mutation spectrum of the CYP21A2 gene. Methods: Families were subjected to clinical, bio...

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Библиографические подробности
Главные авторы: Rabbani, Bahareh, Mahdieh, Nejat, Ashtiani, Mohammad Tahgi Haghi, Larijani, Bagher, Akbari, Mohammad Taghi, New, Maria, Parsa, Alan, Schouten, Jan P., Rabbani, Ali
Формат: Artigo
Язык:Inglês
Опубликовано: Mary Ann Liebert, Inc. 2012
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Original Articles
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC3277924/
https://ncbi.nlm.nih.gov/pubmed/22017335
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1089/gtmb.2011.0099
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