Genetic Characterization of a Cohort of Italian Patients with Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency

ConclusionThis work, representing a comprehensive genetic study, expanded theCYP21A2 variants spectrum of Italian patients with 21OHD and could be helpful in prenatal diagnosis and genetic counseling.
Source: Molecular Diagnosis and Therapy - Category: Molecular Biology Source Type: research