학술논문

Congenital adrenal hyperplasia due to 11-hydroxylase deficiency: Functional characterization of two novel point mutations and a three-base pair deletion in the CYP11B1 gene
Document Type
Journal
Source
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM; JUN 2005, 90 6, p3724-p3730, 7p.
Subject
Language
English
ISSN
0021972X