Abstract
Studies of families, including twins, show that autoimmune diseases are weakly inherited, with disease specificity, the Mendelian pattern being that of causation by multiple, co-dominant (expressed in the heterozygous state) genes with incomplete penetrance [1]. What genes are these? Before discussing this we need to describe the histocompatibility system.
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Adams, D.D., Adams, C.D. (2013). Genetics. In: Autoimmune Disease. SpringerBriefs in Public Health. Springer, Dordrecht. https://doi.org/10.1007/978-94-007-6937-3_3
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DOI: https://doi.org/10.1007/978-94-007-6937-3_3
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