Whole-exome sequencing identified genes known to be responsible for retinitis pigmentosa in 28 Chinese families

PURPOSE: Retinitis pigmentosa (RP) is a group of highly heterogenetic inherited retinal degeneration diseases. Molecular genetic diagnosis of RP is quite challenging because of the complicated disease-causing mutation spectrum. The aim of this study was to explore the mutation spectrum in Chinese RP...

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Detalles Bibliográficos
Autores principales: Shen, Chang, You, Bing, Chen, Yu-Ning, Li, Yang, Li, Wei, Wei, Wen-Bin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2022
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9239900/
https://www.ncbi.nlm.nih.gov/pubmed/35814500

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9239900/
https://www.ncbi.nlm.nih.gov/pubmed/35814500

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