TNFAIP3 Gene Polymorphisms in a Chinese Han Population with Vogt–Koyanagi–Harada Syndrome

BACKGROUND: This study was performed to evaluate the potential association of TNFAIP3 polymorphisms with Vogt–Koyanagi–Harada (VKH) disease in a Chinese Han population. METHODOLOGY/PRINCIPAL FINDINGS: Five single-nucleotide polymorphisms (SNPs), rs10499194, rs610604, rs7753873, rs5029928 and rs94948...

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Autores principales: Li, Hong, Liu, Qing, Hou, Shengping, Du, Liping, Zhou, Qingyun, Zhou, Yan, Kijlstra, Aize, Yang, Peizeng
Formato: Artigo
Lenguaje:Inglês
Publicado: Public Library of Science 2013
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Research Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC3605404/
https://ncbi.nlm.nih.gov/pubmed/23555688
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0059515
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