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.
Guardat en:
| Publicat a: | J Clin Invest |
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| Autors principals: | , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
American Society for Clinical Investigation
1981
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC370603/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/7462431/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI110070 |
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