Molecular Analysis of CYP21A2 Gene Mutations among Congenital Adrenal Hyperplasia Patients in Iraq

A category of autosomal recessive illnesses known as congenital adrenal hyperplasia. 21-hydroxylase insufficiency is the most common. Iraq has yet to report on the analysis of CYP21A2 gene mutations. The goal of this study is to look at the range

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