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Epigenome-wide association study identifies Vogt-Koyanagi-Harada disease-associated DNA methylation loci in Chinese.
Su, Guannan; Du, Liping; Yu, Hongsong; Li, Minghui; Huang, Ruocheng; Yang, Xiaonan; Wang, Detao; Wang, Qing; Yang, Peizeng.
  • Su G; The First Affiliated Hospital of Chongqing Medical University, Chongqing Key Laboratory of Ophthalmology, Chongqing Eye Institute, Chongqing Branch (Municipality Division) of National Clinical Research Center for Ocular Diseases, Chongqing, China.
  • Du L; Department of Ophthalmology, The First Affiliated Hospital of Zhengzhou University, Henan Province Eye Hospital, Henan International Joint Research Laboratory for Ocular Immunology and Retinal Injury Repair, Zhengzhou, China.
  • Yu H; The First Affiliated Hospital of Chongqing Medical University, Chongqing Key Laboratory of Ophthalmology, Chongqing Eye Institute, Chongqing Branch (Municipality Division) of National Clinical Research Center for Ocular Diseases, Chongqing, China.
  • Li M; Sinotech Genomics Ltd, Shanghai, 210000, China.
  • Huang R; Sinotech Genomics Ltd, Shanghai, 210000, China.
  • Yang X; Sinotech Genomics Ltd, Shanghai, 210000, China.
  • Wang D; Shanghai Biotechnology Corporation, Shanghai, China.
  • Wang Q; Shanghai Biotechnology Corporation, Shanghai, China.
  • Yang P; The First Affiliated Hospital of Chongqing Medical University, Chongqing Key Laboratory of Ophthalmology, Chongqing Eye Institute, Chongqing Branch (Municipality Division) of National Clinical Research Center for Ocular Diseases, Chongqing, China. Electronic address: peizengycmu@126.com.
Exp Eye Res ; 233: 109553, 2023 08.
Article en En | MEDLINE | ID: mdl-37394087
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Síndrome Uveomeningoencefálico / Metilación de ADN Tipo de estudio: Risk_factors_studies Límite: Humans Idioma: En Año: 2023 Tipo del documento: Article
Texto completo
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XML
PubMed Links
Search on Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Síndrome Uveomeningoencefálico / Metilación de ADN Tipo de estudio: Risk_factors_studies Límite: Humans Idioma: En Año: 2023 Tipo del documento: Article