Ocular Features and Mutation Spectrum of Patients With Familial Exudative Vitreoretinopathy

PURPOSE: To investigate the clinical findings in Chinese patients diagnosed with familial exudative vitreoretinopathy (FEVR) and carrying pathogenic mutations. METHODS: One hundred twenty unrelated patients with FEVR were enrolled in this study. Genomic DNA and ophthalmic examinations were collected...

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Detalles Bibliográficos
Autores principales: Tao, Tianchang, Xu, Ningda, Li, Jiarui, Li, Hongyan, Qu, Jinfeng, Yin, Hong, Liang, Jianhong, Zhao, Mingwei, Li, Xiaoxin, Huang, Lvzhen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Association for Research in Vision and Ophthalmology 2021
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8648064/
https://www.ncbi.nlm.nih.gov/pubmed/34860240
http://dx.doi.org/10.1167/iovs.62.15.4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8648064/
https://www.ncbi.nlm.nih.gov/pubmed/34860240
http://dx.doi.org/10.1167/iovs.62.15.4

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