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Genome-wide association analysis of Vogt-Koyanagi-Harada syndrome identifies two new susceptibility loci at 1p31.2 and 10q21.3.
Hou S, Du L, Lei B, Pang CP, Zhang M, Zhuang W, Zhang M, Huang L, Gong B, Wang M, Zhang Q, Hu K, Zhou Q, Qi J, Wang C, Tian Y, Ye Z, Liang L, Yu H, Li H, Zhou Y, Cao Q, Liu Y, Bai L, Liao D, Kijlstra A, Xu J, Yang Z, Yang P. Hou S, et al. Among authors: wang m, wang c. Nat Genet. 2014 Sep;46(9):1007-11. doi: 10.1038/ng.3061. Epub 2014 Aug 10. Nat Genet. 2014. PMID: 25108386
Macular Abnormalities in Vogt-Koyanagi-Harada Disease.
Yang P, Ye Z, Xu J, Du L, Zhou Q, Qi J, Liang L, Wang C, Zhou C, Cao Q, Wu L, Kijlstra A. Yang P, et al. Among authors: wang c. Ocul Immunol Inflamm. 2019;27(8):1195-1202. doi: 10.1080/09273948.2019.1624781. Epub 2019 Aug 15. Ocul Immunol Inflamm. 2019. PMID: 31415220
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