Valine

cytochrome P450 family 21 subfamily A member 2 ; Homo sapiens







4 Article(s)
Download
PMID
Title
Pub. Year
#Total Relationships
1 9579234 Carrier status for steroid 21-hydroxylase deficiency is only one factor in the variable phenotype of acne. 1998 Feb 1
2 2226916 Late onset adrenal hyperplasia: mutation at codon 282 of the functional 21-hydroxylase gene is not ubiquitous. 1990 Nov 1
3 2788081 Clinical and genetic characterization of nonclassic 21-hydroxylase deficiency. 1989 2
4 3260007 Molecular genetic analysis of nonclassic steroid 21-hydroxylase deficiency associated with HLA-B14,DR1. 1988 Jul 7 2