Substitutions in the CYP21A2 promoter explain the simple-virilizing form of 21-hydroxylase deficiency in patients harbouring a P30L mutation - Araujo, Rogério S.; Billerbeck, Ana Elisa C.; Madureira, Guiomar; Mendonça, Berenice Bilharinho; Bachega, Tânia A. S. S. (Clinical Endocrinology, 2005)