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  - Grötzinger 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  - 2024/12/21

ER  -