Molecular Analysis of CYP21A2 Gene Mutations among Iraqi Patients with Congenital Adrenal Hyperplasia

Congenital adrenal hyperplasia is a group of autosomal recessive disorders. The most frequent one is 21-hydroxylase deficiency. Analyzing CYP21A2 gene mutations was so far not reported in Iraq. This work aims to analyze the spectrum and frequency of CYP21A2 mutations among Iraqi CAH patients. Sixty-...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Enzyme Res
Prif Awduron: Al-Obaidi, Ruqayah G. Y., Al-Musawi, Bassam M. S., Al-Zubaidi, Munib Ahmed K., Oberkanins, Christian, Németh, Stefan, Al-Obaidi, Yusra G. Y.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Hindawi Publishing Corporation 2016
Pynciau:
Research Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC5061977/
https://ncbi.nlm.nih.gov/pubmed/27777794
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2016/9040616
Tagiau: Ychwanegu Tag
Dim Tagiau, Byddwch y cyntaf i dagio'r cofnod hwn!

Eitemau Tebyg