Retinal Features of Family Members With Familial Exudative Vitreoretinopathy Caused By Mutations in KIF11 Gene

PURPOSE: To determine the clinical characteristics of patients and family members with familial exudative vitreoretinopathy (FEVR) caused by mutations in the KIF11 gene. METHODS: Twenty-one patients from 10 FEVR families with mutations in the KIF11 gene were studied. The retinal and systemic feature...

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Detalles Bibliográficos
Autores principales: Kondo, Hiroyuki, Matsushita, Itsuka, Nagata, Tatsuo, Fujihara, Etsuko, Hosono, Katsuhiro, Uchio, Eiichi, Hotta, Yoshihiro, Kusaka, Shunji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Association for Research in Vision and Ophthalmology 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8212440/
https://www.ncbi.nlm.nih.gov/pubmed/34128965
http://dx.doi.org/10.1167/tvst.10.7.18

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