Complement-human histocompatibility antigen haplotypes in C2 deficiency
- PMID: 7462431
- PMCID: PMC370603
- DOI: 10.1172/JCI110070
Complement-human histocompatibility antigen haplotypes in C2 deficiency
Abstract
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.
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