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Correlation between FBN1 mutations and ocular features with ectopia lentis in the setting of Marfan syndrome and related fibrillinopathies.
Chen, Ze-Xu; Chen, Tian-Hui; Zhang, Min; Chen, Jia-Hui; Lan, Li-Na; Deng, Michael; Zheng, Jia-Lei; Jiang, Yong-Xiang.
Afiliação
  • Chen ZX; Eye Institute and Department of Ophthalmology, Eye & ENT Hospital, Fudan University, Shanghai, China.
  • Chen TH; NHC Key Laboratory of Myopia (Fudan University), Key Laboratory of Myopia, Chinese Academy of Medical Sciences, Shanghai, China.
  • Zhang M; Shanghai Key Laboratory of Visual Impairment and Restoration, Shanghai, China.
  • Chen JH; Eye Institute and Department of Ophthalmology, Eye & ENT Hospital, Fudan University, Shanghai, China.
  • Lan LN; NHC Key Laboratory of Myopia (Fudan University), Key Laboratory of Myopia, Chinese Academy of Medical Sciences, Shanghai, China.
  • Deng M; Shanghai Key Laboratory of Visual Impairment and Restoration, Shanghai, China.
  • Zheng JL; Eye Institute and Department of Ophthalmology, Eye & ENT Hospital, Fudan University, Shanghai, China.
  • Jiang YX; NHC Key Laboratory of Myopia (Fudan University), Key Laboratory of Myopia, Chinese Academy of Medical Sciences, Shanghai, China.
Hum Mutat ; 42(12): 1637-1647, 2021 12.
Article em En | MEDLINE | ID: mdl-34550612
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ectopia do Cristalino / Síndrome de Marfan Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ectopia do Cristalino / Síndrome de Marfan Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article