Two Prevalent CYP17 Mutations and Genotype-Phenotype Correlations in 24 Brazilian Patients with 17-Hydroxylase Deficiency

Article

Abstract: We performed molecular genetic analysis of 24 subjects from 19 families with 17-hydroxylase deficien

Palabras claves:

Autores:

Costa-Santos M., Kater C.E., Richard J. Auchus

Fuentes:

scopus