RPE65 mutation frequency and phenotypic variation according to exome sequencing in a tertiary centre for genetic eye diseases in China

PURPOSE: Retinoid isomerohydrolase RPE65 has received a tremendous amount of attention due to successful clinical gene therapy for Leber congenital amaurosis (LCA) cases caused by RPE65 mutations. This study aimed to evaluate the frequency of RPE65 mutations and the associated phenotypes based on ex...

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Detalles Bibliográficos
Autores principales: Li, Shiqiang, Xiao, Xueshan, Yi, Zhen, Sun, Wenmin, Wang, Panfeng, Zhang, Qingjiong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7079156/
https://www.ncbi.nlm.nih.gov/pubmed/31273949
http://dx.doi.org/10.1111/aos.14181

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7079156/
https://www.ncbi.nlm.nih.gov/pubmed/31273949
http://dx.doi.org/10.1111/aos.14181

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