Association of a TNIP1 Polymorphism with Vogt-Koyanagi-Harada Syndrome but Not with Ocular Behcet’s Disease in Han Chinese

OBJECTIVES: The aim of the study was to investigate the association of TNFα-induced protein 3 interacting with protein 1 (TNIP1) gene polymorphisms with Vogt–Koyanagi–Harada (VKH) syndrome and Behcet’s disease (BD) in a Han Chinese population. METHODS: A total of 656 BD patients, 961 VKH syndrome pa...

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Detalles Bibliográficos
Autores principales: Shi, Yanyun, Jia, Yading, Hou, Shengping, Fang, Jing, Zhou, Yan, Kijlstra, Aize, Yang, Peizeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4008420/
https://www.ncbi.nlm.nih.gov/pubmed/24788730
http://dx.doi.org/10.1371/journal.pone.0095573

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4008420/
https://www.ncbi.nlm.nih.gov/pubmed/24788730
http://dx.doi.org/10.1371/journal.pone.0095573

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