Evaluation of PTPN22 polymorphisms and Vogt-Koyanagi-Harada disease in Japanese patients

PURPOSE: Vogt-Koyanagi-Harada (VKH) disease is an autoimmune disorder against melanocytes. Polymorphisms of the protein tyrosine phosphatase non-receptor 22 gene (PTPN22) have recently been reported to be associated with susceptibility to several autoimmune diseases. In this study, genetic susceptib...

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Main Authors: Horie, Yukihiro, Kitaichi, Nobuyoshi, Katsuyama, Yoshihiko, Yoshida, Kazuhiko, Miura, Toshie, Ota, Masao, Asukata, Yuri, Inoko, Hidetoshi, Mizuki, Nobuhisa, Ishida, Susumu, Ohno, Shigeaki
Formato: Artigo
Idioma:Inglês
Publicado: Molecular Vision 2009
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Research Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC2690962/
https://ncbi.nlm.nih.gov/pubmed/19503742
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