Phenotype-genotype correlations of 13 rare CYP21A2 mutations detected in 46 patients affected with 21-hydroxylase deficiency and in one carrier - Tardy, V; Menassa, R; Sulmont, V; Lienhardt-Roussie, A; Lecointre, C; Brauner, R; David, M; Morel, Y (J Clin Endocrinol Metab, 2010)