Single nucleotide polymorphism study of IDDM 17 in a Bedouin Arab family

Ann N Y Acad Sci. 2003 Nov:1005:348-51. doi: 10.1196/annals.1288.056.

Abstract

Type 1 diabetes is an autoimmune disease caused by a combination of genetic and environmental factors. On the basis of a genomic search for linkage in a Bedouin Arab family with 19 members with type 1 diabetes, we previously mapped the IDDM 17 locus to the chromosome 10q25.1 region. The result from a recent genome scan showed suggestive evidence of linkage of IDDM 17 in a subset of Caucasian families in which all affected individuals have DR3, indicating that the IDDM 17 locus might have a measurable effect in Caucasian populations from the United Kingdom and the United States. High-resolution SNP typing provides strong evidence of linkage disequilibrium to the IDDM 17 locus.

MeSH terms

  • Arabs
  • Chromosomes, Human, Pair 10
  • Diabetes Mellitus, Type 1 / ethnology
  • Diabetes Mellitus, Type 1 / genetics*
  • Humans
  • Linkage Disequilibrium
  • Polymorphism, Single Nucleotide*