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...

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Vydáno v:Adv Biomed Res
Hlavní autoři: Kolahdouz, Mahsa, Hashemipour, Mahin, Khanahmad, Hossein, Rabbani, Bahareh, Salehi, Mansoor, Rabbani, Ali, Ansari, Arman, Naseri, Mona Mobalegh
Médium: Artigo
Jazyk:Inglês
Vydáno: Medknow Publications & Media Pvt Ltd 2016
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Original Article
On-line přístup: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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