The association of the PTPN22 620W polymorphism with Behçet's disease

OBJECTIVES: A single nucleotide polymorphism (SNP) of the gene encoding protein tyrosine phosphatase type 22 (PTPN22 620W) has recently been described as a strong common genetic risk factor for human autoimmune disease. We have analysed the association of PTPN22 620W in patients with Behçet's d...

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Bibliografski detalji
Glavni autori: Baranathan, Vijay, Stanford, Miles R, Vaughan, Robert W, Kondeatis, Elli, Graham, Elizabeth, Fortune, Farida, Madanat, Wafa, Kanawati, Charlie, Ghabra, Marwen, Murray, Philip I, Wallace, Graham R
Format: Artigo
Jezik:Inglês
Izdano: BMJ Group 2007
Teme:
Concise Report
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC2111602/
https://ncbi.nlm.nih.gov/pubmed/17660222
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/ard.2007.073866
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