Polymorphism of the Second Component of Complement (C2) in Graves’ Disease
- 1 January 1980
- journal article
- research article
- Published by S. Karger AG in Human Heredity
- Vol. 30 (4), 245-247
- https://doi.org/10.1159/000153136
Abstract
The polymorphism of C2 was studied by isoelectric focussing in 60 patients with Graves’ disease and compared to 8001 control sera. No difference in gene frequencies was observed.Keywords
This publication has 4 references indexed in Scilit:
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- Mapping of the HLA locus controlling C2 structural variants and linkage disequilibrium between alleles C22 and Bw15European Journal of Immunology, 1976
- Inherited structural polymorphism in human C2: evidence for genetic linkage between C2 and Bf.The Journal of Experimental Medicine, 1976
- The Association of HLA with Autoimmune Thyroid Disease in Newfoundland. The Influence of HLA Homozygosity in Graves’ DiseaseTissue Antigens, 1976