No evidence for association of PTPN22 R620W functional variant C1858T with type 1 diabetes in Asian Indians

Ítems similars

• The PTPN22 C1858T (R620W) functional polymorphism in inflammatory bowel disease
  per: Zaid, Younes, et al.
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• The R620W Polymorphism of the Protein Tyrosine Phosphatase PTPN22 Is Not Associated with Multiple Sclerosis
  per: Begovich, Ann B., et al.
  Publicat: (2005)
• Identification of the PTPN22 functional variant R620W as susceptibility genetic factor for giant cell arteritis
  per: Serrano, A, et al.
  Publicat: (2013)
• The PTPN22 allele encoding an R620W variant interferes with the removal of developing autoreactive B cells in humans
  per: Menard, Laurence, et al.
  Publicat: (2011)
• The Protein Tyrosine Phosphatase Nonreceptor 22 (PTPN22) R620W Functional Polymorphism in Psoriasis
  per: Bin Huraib, Ghaleb, et al.
  Publicat: (2018)