Authors:
Dardis, A
Marino, R
Bergada, I
Escobar, ME
Gryngarten, M
Rivarola, MA
Belgorosky, A
Citation: A. Dardis et al., Molecular analysis of the most frequent mutations associated with congenital adrenal hyperplasia secondary to steroid 21-hydroxylase enzyme deficiency, MEDICINA, 61(1), 2001, pp. 28-34