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A Novel Human Congenital Cataract Mutation in EPHA2 Kinase Domain (p.G668D) Alters Receptor Stability and Function.
Zhai, Yi; Zhu, Sha; Li, Jinyu; Yao, Ke.
Afiliação
  • Zhai Y; Department of Ophthalmology and Visual Sciences, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Alberta, Canada.
  • Zhu S; Eye Center, the Second Affiliated Hospital of the School of Medicine, Zhejiang University, Hangzhou, Zhejiang, People's Republic of China.
  • Li J; Eye Center, the Second Affiliated Hospital of the School of Medicine, Zhejiang University, Hangzhou, Zhejiang, People's Republic of China.
  • Yao K; Eye Center, the Second Affiliated Hospital of the School of Medicine, Zhejiang University, Hangzhou, Zhejiang, People's Republic of China.
Invest Ophthalmol Vis Sci ; 60(14): 4717-4726, 2019 11 01.
Article em En | MEDLINE | ID: mdl-31725171
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Catarata / Mutação de Sentido Incorreto / Receptor EphA2 / Efrina-A2 Idioma: En Ano de publicação: 2019 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Catarata / Mutação de Sentido Incorreto / Receptor EphA2 / Efrina-A2 Idioma: En Ano de publicação: 2019 Tipo de documento: Article