The coexistence of IgA deficiency and 21-hydroxylase deficiency marked by specific MHC supratypes.

Annals of the New York Academy of Sciences ·Vol. 458 ·1985-00-00 ·Pages 76-84

Cobain TJ, Stuckey MS, McCluskey J, Wilton AN, Gedeon A, Garlepp MJ, Christiansen FT, Dawkins RL

Abstract

暂无摘要

MeSH Terms

Adrenal Hyperplasia, Congenital/genetics Chromosome Mapping Dysgammaglobulinemia/genetics Female Genetic Carrier Screening Genotype HLA Antigens/genetics HLA-A Antigens HLA-B Antigens HLA-DR Antigens Histocompatibility Antigens Class II/genetics Histocompatibility Testing Humans IgA Deficiency Major Histocompatibility Complex Male Pedigree Steroid Hydroxylases/deficiency

Chemicals

HLA Antigens HLA-A Antigens HLA-B Antigens HLA-DR Antigens Histocompatibility Antigens Class II Steroid Hydroxylases

Authors & Affiliations

8 authors, click to expand affiliations / ORCID

Cobain T J

Stuckey M S

McCluskey J

Wilton A N

Gedeon A

Garlepp M J

Christiansen F T

Dawkins R L

Article Info

Journal

Annals of the New York Academy of Sciences

Abbr.

Ann N Y Acad Sci

ISSN

0077-8923

DOI

10.1111/j.1749-6632.1985.tb14593.x

Published

1985-00-00

Pages

76-84

Language

English

Region

United States

NLM ID

7506858

Subset

External Links

PubMed source DOI: 10.1111/j.1749-6632.1985.tb14593.x View journal details

Analysis Services

The coexistence of IgA deficiency and 21-hydroxylase deficiency marked by specific MHC supratypes.

Contact

WeChat Official Account