首页> 外文期刊>British journal of ophthalmology >Investigation of the association of Vogt-Koyanagi-Harada syndrome with IL23R-C1orf141 in Han Chinese Singaporean and ADO-ZNF365-EGR2 in Thai
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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

机译:Vogt-Koyanagi-Harada综合征与新加坡汉族人IL23R-C1orf141和泰国人ADO-ZNF365-EGR2的关联调查

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摘要

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-ZNF365EGR2 with VKH syndrome in four sets of multinational populations in Asia.
机译:背景我们在汉族人群中进行了Vogt-Koyanagi-Harada(VKH)综合征的多阶段全基因组关联研究,并先前鉴定了两个新的非人类白细胞抗原候选区域。该研究的目的是在亚洲的四组跨国人群中复制IL23R-C1orf141和ADO-ZNF365EGR2与VKH综合征的关联。

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