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Linkage disequilibria between HLA-B and the rarer properdin factor B alleles, BfF1 and BfS1
Authors:G.J. Stewart  H.M. Cann  F.C. Grumet  R. Hay  R.L. Kirk  R. Payne
Affiliation:1. Department of Medicine, Pediatrics, Genetics, and Pathology, Stanford University School of Medicine, Stanford, California, USA;2. South Australian Red Cross Blood Transfusion Service, Adelaide, Australia;3. Department of Human Biology, John Curtin School of Medical Research, Canberra, Australia
Abstract:
Phenotypic association and highly significant linkage disequilibria have been demonstrated for HLA-B18 and BfF1 and HLA-Bw50 and BfS1 alleles among Caucasians from Australia and the United States (San Francisco Bay area). The HLA-B18, BfuF1 association appears to be associated with HLA-Aw30. It is possible that BfS1 as a mutation, after the evolutionary splitting of HLA-Bw21, on an HLA-Bw50 haplotype, and that BfF1 arose on an HLA-Aw30, B18 haplotype.
Keywords:Bf  properdin factor B  IDDM  insulin dependent diabetes mellitus  LD  linkage disequilibrium
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