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-...

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Gepubliceerd in:Enzyme Res
Hoofdauteurs: Al-Obaidi, Ruqayah G. Y., Al-Musawi, Bassam M. S., Al-Zubaidi, Munib Ahmed K., Oberkanins, Christian, Németh, Stefan, Al-Obaidi, Yusra G. Y.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Hindawi Publishing Corporation 2016
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Research Article
Online toegang: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
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