Evaluation of PTPN22 polymorphisms and Vogt-Koyanagi-Harada disease in Japanese patients.
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Association of a TNIP1 polymorphism with Vogt-Koyanagi-Harada syndrome but not with ocular Behcet's disease in Han Chinese.A functional variant of PTPN22 confers risk for Vogt-Koyanagi-Harada syndrome but not for ankylosing spondylitis.Influence of molecular genetics in Vogt-Koyanagi-Harada disease.
P2860
Evaluation of PTPN22 polymorphisms and Vogt-Koyanagi-Harada disease in Japanese patients.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 03 June 2009
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Evaluation of PTPN22 polymorphisms and Vogt-Koyanagi-Harada disease in Japanese patients.
@en
Evaluation of PTPN22 polymorphisms and Vogt-Koyanagi-Harada disease in Japanese patients.
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type
label
Evaluation of PTPN22 polymorphisms and Vogt-Koyanagi-Harada disease in Japanese patients.
@en
Evaluation of PTPN22 polymorphisms and Vogt-Koyanagi-Harada disease in Japanese patients.
@nl
prefLabel
Evaluation of PTPN22 polymorphisms and Vogt-Koyanagi-Harada disease in Japanese patients.
@en
Evaluation of PTPN22 polymorphisms and Vogt-Koyanagi-Harada disease in Japanese patients.
@nl
P2093
P2860
P1433
P1476
Evaluation of PTPN22 polymorphisms and Vogt-Koyanagi-Harada disease in Japanese patients
@en
P2093
Hidetoshi Inoko
Kazuhiko Yoshida
Nobuhisa Mizuki
Nobuyoshi Kitaichi
Shigeaki Ohno
Susumu Ishida
Toshie Miura
Yoshihiko Katsuyama
Yukihiro Horie
P2860
P304
P577
2009-06-03T00:00:00Z