학술논문
A mutation (Pro-30 to Leu) in CYP21 represents a potential nonclassic steroid 21-hydroxylase deficiency allele
Document Type
Article
Author
Source
In: Molecular Endocrinology . (Molecular Endocrinology, May 1991, 5(5):685-692)
Subject
Language
English
ISSN
08888809