Associated Papers
Challenging Molecular Diagnosis of Congenital Adrenal Hyperplasia (CAH) Due to 21-Hydroxylase Deficiency: Case Series and Novel Variants of CYP21A2 Gene.
Concolino P
Current Issues in Molecular Biology, 2024
Mutation analysis of the CYP21A2 gene in congenital adrenal hyperplasia.
Forouzanfar K et al.
Cellular and Molecular Biology (noisy-le-grand, France), 2015
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