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pubmed-article:7813807pubmed:abstractTextType I diabetes susceptibility genes have been identified within the major histocompatibility complex (MHC) on chromosome 6p21.3 and near the VNTR/insulin region on chromosome 11p15.5. We have used polymorphic dinucleotide repeat markers to search the human genome for additional susceptibility genes in 162 type I diabetic families with an affected sibling pair. We report that an additional susceptibility gene is located on chromosome 2q31 near HOXD8 (P < 10(-5), maximum logarithm of odds score = 4.8) in an analysis of affected sibling pairs having specific human leukocyte antigen (HLA) and hypervariable nucleotide tandem repeat (VNTR)/insulin gene haplotypes (absence of high-risk HLA-DR3/4 haplotypes and presence of homozygous high-risk class I VNTR alleles). These results suggest the interaction of a minimum of three genes in the pathogenesis of type I diabetes in humans.lld:pubmed
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pubmed-article:7813807pubmed:pagination132-6lld:pubmed
pubmed-article:7813807pubmed:dateRevised2010-11-18lld:pubmed
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pubmed-article:7813807pubmed:articleTitleThe HOXD8 locus (2q31) is linked to type I diabetes. Interaction with chromosome 6 and 11 disease susceptibility genes.lld:pubmed
pubmed-article:7813807pubmed:affiliationDepartment of Pediatrics, Baylor College of Medicine, Houston, TX 77030.lld:pubmed
pubmed-article:7813807pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:7813807pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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