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Investigation of the association of Vogt-Koyanagi-Harada syndrome with IL23R-C1orf141 in Han Chinese Singaporean and ADO-ZNF365-EGR2 in Thai.

The British journal of ophthalmology - 1 Mar 2016

Cao Shuang, Chee Soon Phaik, Yu Hyeong Gon, Sukavatcharin Somsiri, Wu Lili, Kijlstra Aize, Hou Shengping, Yang Peizeng

Abstract excerpt

BACKGROUND: We performed a multistage genome-wide association study of Vogt-Koyanagi-Harada (VKH) syndrome in a Han Chinese population and identified two novel non-human leukocyte antigen candidate regions previously. The aim of the study was to replicate the association of IL23R-C1orf141 and ADO-ZNF365-EGR2 with VKH syndrome in four sets of multinational populations in Asia. METHOD: We conducted a candidate...

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Identifiers

PMID: 26628628
DOI: 10.1136/bjophthalmol-2015-307366

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ADO
EGR2

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