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...

Full description

Saved in:
Bibliographic Details
Published in:Adv Biomed Res
Main Authors: Kolahdouz, Mahsa, Hashemipour, Mahin, Khanahmad, Hossein, Rabbani, Bahareh, Salehi, Mansoor, Rabbani, Ali, Ansari, Arman, Naseri, Mona Mobalegh
Format: Artigo
Language:Inglês
Published: Medknow Publications & Media Pvt Ltd 2016
Subjects:
Original Article
Online Access: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
Tags: Add Tag
No Tags, Be the first to tag this record!

Similar Items