Complement-human histocompatibility antigen haplotypes in C2 deficiency

C4 allotyping 13 homozygous C2-deficient individuals demonstrated 23 of 25 haplotypes to be of the relatively rare type C4A4 B2. This is of the same magnitude as the association of C2Q0 with HLA-DW2/DR2.

Saved in:
Bibliographic Details
Published in:The Journal of clinical investigation 1981-02, Vol.67 (2), p.581-583
Main Authors: Awdeh, Z L, Raum, D D, Glass, D, Agnello, V, Schur, P H, Johnston, Jr, R B, Gelfand, E W, Ballow, M, Yunis, E, Alper, C A
Format: Article
Language:English
Subjects:
Alleles
Complement C2 - deficiency
Complement C2 - genetics
Female
Haploidy
HLA Antigens - genetics
Homozygote
Humans
Male
Citations: Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:C4 allotyping 13 homozygous C2-deficient individuals demonstrated 23 of 25 haplotypes to be of the relatively rare type C4A4 B2. This is of the same magnitude as the association of C2Q0 with HLA-DW2/DR2.
ISSN:0021-9738
DOI:10.1172/JCI110070