Analysis of CYP21 coding polymorphisms in three ethnic populations: Further evidence of nonamplifying CYP21 alleles among whites

Molecular Diagnosis

Volumn 5, Issue 1, 2000, Pages 47-52

  Killeen, Anthony A ^a  

^a UNIVERSITY OF MICHIGAN MEDICAL SCHOOL   (United States)

Author keywords

Allelic frequencies; CYP21; Ethnic populations; Polymorphisms; Steroid 21 hydroxylase

Indexed keywords

GLUCOCORTICOID; MAJOR HISTOCOMPATIBILITY ANTIGEN; MINERALOCORTICOID; RESTRICTION ENDONUCLEASE;

ALLELE; ARTICLE; CAUCASIAN; DISEASE ASSOCIATION; ETHNOLOGY; GENE AMPLIFICATION; GENE FREQUENCY; GENE LOCUS; GENETIC POLYMORPHISM; GENOTYPE; MAJOR HISTOCOMPATIBILITY COMPLEX; POLYMERASE CHAIN REACTION; RACE DIFFERENCE;

EID: 0034060853     PISSN: 10848592     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1084-8592(00)00010-2     Document Type: Article

References (3)

1. Dupont B, Oberfield S, Smithwick E, Lee T, Levine L: Close genetic linkage between HLA and congenital adrenal hyperplasia (21-hydroxylase deficiency). Lancet 1977;2:1309-1311
2. Higashi Y, Yoshioka H, Yamane M, Gotoh O, FujiiKuriyama Y: Complete nucleotide sequence of two steroid 21-hydroxylase genes tandemly arranged in human chromosome: A pseudogene and a genuine gene. Proc Natl Acad Sci USA 1986;83:2841-2845
3. White PC, New MI, Dupont B: Structure of human steroid 21-hydroxylase genes. Proc Natl Acad Sci USA 1986:83:5111-5115