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Article

Association of a TNIP1 polymorphism with Vogt-Koyanagi-Harada syndrome but not with ocular Behcet's disease in Han Chinese.

PloS one - 1 Jan 2014

Shi Yanyun, Jia Yading, Hou Shengping, Fang Jing, Zhou Yan, Kijlstra Aize, Yang Peizeng

Abstract excerpt

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 patients and 1534 healthy controls were included in this two-stage case control study. Seven SNPs, including...

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Identifiers

PMID: 24788730
DOI: 10.1371/journal.pone.0095573
PMCID: PMC4008420

Genes

TNIP1

Provenance

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