TY - JOUR T1 - Functional Characterization of Two Novel Point Mutations in theCYP21Gene Causing Simple Virilizing Forms of Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency JO - The Journal of Clinical Endocrinology & Metabolism PY - 2005/01/01 AU - Krone N AU - Riepe FG AU - Gr枚tzinger J AU - Partsch C-J AU - Sippell WG ED - DO - DOI: 10.1210/jc.2004-0813 PB - The Endocrine Society VL - 90 IS - 1 SP - 445 EP - 454 Y2 - 2025/05/24 ER -