Multiple Sclerosis: Immunogenetic Analyses of Sib-Pair Double Case Families. II. Studies on the Association of Multiple Sclerosis with C2, C4, BF, C3, C6, and GLO Polymorphisms
- 1 March 1983
- journal article
- research article
- Published by Elsevier BV in Immunobiology
- Vol. 164 (2), 160-170
- https://doi.org/10.1016/s0171-2985(83)80007-2
Abstract
No abstract availableThis publication has 27 references indexed in Scilit:
- Complement-human histocompatibility antigen haplotypes in C2 deficiency.JCI Insight, 1981
- Lysis of measles virus-infected cells by the purified cytolytic alternative complement pathway and antibody.The Journal of Experimental Medicine, 1979
- Association of low C2 and C4 serum levels with the HLA-DW2 allele in healthy individuals.The Journal of Experimental Medicine, 1978
- Chido and Rodgers blood groups are distinct antigenic components of human complement C4Nature, 1978
- C2 HYPOCOMPLEMENTÆMIA IN MULTIPLE SCLEROSISThe Lancet, 1976
- Inherited structural polymorphism in human C2: evidence for genetic linkage between C2 and Bf.The Journal of Experimental Medicine, 1976
- Investigations of red cell glyoxalase in recombinant familiesEuropean Journal of Immunology, 1976
- Expression of C4 on Human Lymphoid Cells and Possible Involvement in Immune Recognition PhenomenaScience, 1976
- Neutralization of Sensitized Virus by the Fourth Component of ComplementScience, 1969
- Genetic polymorphism of the third component of human complement (C′3)JCI Insight, 1968