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Sex-specific association of PTPN22 1858T with type 1 diabetes but not with Hashimoto’s thyroiditis or Addison’s disease in the German population
Author(s) -
Heinrich Kahles,
Elizabeth RamosLopez,
Britta Lange,
O Zwermann,
Martín Reincke,
Klaus Badenhoop
Publication year - 2005
Publication title -
european journal of endocrinology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.897
H-Index - 148
eISSN - 1479-683X
pISSN - 0804-4643
DOI - 10.1530/eje.1.02035
Subject(s) - ptpn22 , medicine , thyroiditis , endocrinology , odds ratio , type 1 diabetes , addison's disease , allele , genetic predisposition , diabetes mellitus , genotype , disease , single nucleotide polymorphism , biology , genetics , gene
Endocrine autoimmune disorders share genetic susceptibility loci, causing a disordered T-cell activation and homeostasis (HLA class II genes, CTLA-4). Recent studies showed a genetic variation within the PTPN22 gene to be an additional risk factor.

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