Genotype-phenotype correlation in patients with 21-hydroxylase deficiency
Introduction21-hydroxylase deficiency (21OHD) is the most common cause of congenital adrenal hyperplasia (CAH).However, patients with 21OHD manifest various phenotypes due to Set Of Three Dip Bowls a wide-spectrum residual enzyme activity of different CYP21A2 mutations.MethodsA total of 15 individuals from three unrelated families were included in