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

Author:

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

Publisher

BMJ

Subject

Cellular and Molecular Neuroscience,Sensory Systems,Ophthalmology

Reference38 articles.

1. Clinical characteristics of Vogt-Koyanagi-Harada syndrome in Chinese patients;Yang;Ophthalmology,2007

2. Vogt-Koyanagi-Harada disease: clinical outcomes;Bykhovskaya;Am J Ophthalmol,2005

3. Vogt-Koyanagi-Harada syndrome;Rao;Int Ophthalmol Clin,1995

4. Tyrosinase gene family and Vogt-Koyanagi-Harada disease in Japanese patients;Horie;Mol Vis,2006

5. [Association of HLA-DQA1 and DQB1 alleles with Vogt-Koyanagi-Harada syndrome in Han Chinese population];Liu;Zhonghua Yan Ke Za Zhi,1999

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