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Evaluation of PTPN22 polymorphisms and Vogt-Koyanagi-Harada disease in Japanese patients
Molecular Vision, 06/05/09
Horie Y et al. - The six SNPs in PTPN22 showed no significant association with susceptibility to VKH disease or its ocular, neurologic, or dermatological manifestation.
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MTHFR gene C677T and A1298C polymorphisms and homocysteine levels in primary open angle and primary closed angle glaucoma
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