A high rate of novel CYP11B1 mutations in Saudi Arabia

Article

Abstract: Despite ethnic variation, 11 β-hydroxylase deficiency (11β-OHD) has generally been considered the se

Palabras claves:

Ambiguous genitalia, Congenital adrenal hyperplasia, CYP11B1, Mutations

Autores:

Al-Sagheir A., Alhomaidah D., Alswailem M., Alzahrani A., Alzahrani O., Bin-Abbas B., Capper C.P., Murugan A., Qasem E., Richard J. Auchus

Fuentes:

scopus