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PMID: 6980755 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Complement C4 allotypes in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: further evidence for different allelic variants at the 21-hydroxylase locus.

Clinical immunology and immunopathology ·Vol. 23 ·No. 2 ·1982-05-00 ·Pages 312-22

O'Neill GJ, Dupont B, Pollack MS, Levine LS, New MI

Abstract

暂无摘要

MeSH Terms
Adrenal Hyperplasia, Congenital/genetics,immunology Alleles Chromosome Mapping Complement C4/genetics Complement C4a Gene Frequency Genetic Variation Genotype HLA Antigens/genetics Haploidy Humans Steroid 21-Hydroxylase/genetics Steroid Hydroxylases/deficiency
Chemicals
Complement C4 HLA Antigens Complement C4a Steroid Hydroxylases Steroid 21-Hydroxylase
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
O'Neill G J
Dupont B
Pollack M S
Levine L S
New M I
Article Info
Journal
Clinical immunology and immunopathology
Abbr.
Clin Immunol Immunopathol
ISSN
0090-1229
DOI
10.1016/0090-1229(82)90117-9
Published
1982-05-00
Pages
312-22
Language
English
Region
United States
NLM ID
0356637
Subset
IM
Grants
NCI NIH HHS · CA 08747 · United States
NCI NIH HHS · CA 19267 · United States
NCI NIH HHS · CA 22507 · United States
External Links
PubMed source DOI: 10.1016/0090-1229(82)90117-9
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