Loading...

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...

Fuld beskrivelse

Na minha lista:
Bibliografiske detaljer
Main Authors: Shi, Yanyun, Jia, Yading, Hou, Shengping, Fang, Jing, Zhou, Yan, Kijlstra, Aize, Yang, Peizeng
Format: Artigo
Sprog:Inglês
Udgivet: Public Library of Science 2014
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4008420/
https://ncbi.nlm.nih.gov/pubmed/24788730
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0095573
Tags: Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!