Mutation detection of CYP21A2 gene in nonclassical congenital adrenal hyperplasia patients with premature pubarche

BACKGROUND: Congenital adrenal hyperplasia (CAH) due to mutations in the gene encoding 21-hydroxilase is one of common disease with an autosomal recessive form. In this study, our aim is to detect the prevalence of eight common mutations in nonclassical congenital adrenal hyperplasia (NCAH). MATERIA...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Adv Biomed Res
Prif Awduron: Kolahdouz, Mahsa, Hashemipour, Mahin, Khanahmad, Hossein, Rabbani, Bahareh, Salehi, Mansoor, Rabbani, Ali, Ansari, Arman, Naseri, Mona Mobalegh
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Medknow Publications & Media Pvt Ltd 2016
Pynciau:
Original Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC4815525/
https://ncbi.nlm.nih.gov/pubmed/27099846
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/2277-9175.178794
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