Mutation Analysis in Patients with Congenital Adrenal Hyperplasia in the Spanish Population: Identification of Putative Novel Steroid 21-Hydroxylase Deficiency Alleles Associated with the Classic Form of the Disease
Lobato, M. Natividad, Ordóñez-Sánchez, M. Luisa, Tusié-Luna, M. Teresa, Meseguer, AnnaVolume:
49
Language:
english
Journal:
Human Heredity
DOI:
10.1159/000022866
Date:
May, 1999
File:
PDF, 452 KB
english, 1999