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Association of a NOS3 gene polymorphism with Behçet's disease but not with Vogt-Koyanagi-Harada syndrome in Han Chinese.
Zhou, Yan; Yu, Hongsong; Hou, Shengping; Fang, Jing; Qin, Jieying; Yuan, Gangxiang; Kijlstra, Aize; Yang, Peizeng.
Afiliação
  • Zhou Y; The First Affiliated Hospital of Chongqing Medical University, Chongqing Key Laboratory of Ophthalmology and Chongqing Eye Institute, Chongqing, P. R. China; Department of Ophthalmology, Yongchuan Hospital, Chongqing Medical University, Chongqing, China.
  • Yu H; The First Affiliated Hospital of Chongqing Medical University, Chongqing Key Laboratory of Ophthalmology and Chongqing Eye Institute, Chongqing, P. R. China.
  • Hou S; The First Affiliated Hospital of Chongqing Medical University, Chongqing Key Laboratory of Ophthalmology and Chongqing Eye Institute, Chongqing, P. R. China.
  • Fang J; The First Affiliated Hospital of Chongqing Medical University, Chongqing Key Laboratory of Ophthalmology and Chongqing Eye Institute, Chongqing, P. R. China.
  • Qin J; The First Affiliated Hospital of Chongqing Medical University, Chongqing Key Laboratory of Ophthalmology and Chongqing Eye Institute, Chongqing, P. R. China.
  • Yuan G; The First Affiliated Hospital of Chongqing Medical University, Chongqing Key Laboratory of Ophthalmology and Chongqing Eye Institute, Chongqing, P. R. China.
  • Kijlstra A; University Eye Clinic Maastricht, Maastricht, The Netherlands.
  • Yang P; The First Affiliated Hospital of Chongqing Medical University, Chongqing Key Laboratory of Ophthalmology and Chongqing Eye Institute, Chongqing, P. R. China.
Mol Vis ; 22: 311-8, 2016.
Article em En | MEDLINE | ID: mdl-27114698
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Síndrome Uveomeningoencefálica / Síndrome de Behçet / Polimorfismo de Nucleotídeo Único / Povo Asiático / Óxido Nítrico Sintase Tipo III Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male País/Região como assunto: Asia Idioma: En Revista: Mol Vis Assunto da revista: BIOLOGIA MOLECULAR / OFTALMOLOGIA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: China
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Síndrome Uveomeningoencefálica / Síndrome de Behçet / Polimorfismo de Nucleotídeo Único / Povo Asiático / Óxido Nítrico Sintase Tipo III Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male País/Região como assunto: Asia Idioma: En Revista: Mol Vis Assunto da revista: BIOLOGIA MOLECULAR / OFTALMOLOGIA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: China