CRISPR DNA Base Editing Strategies for Treating Retinitis Pigmentosa Caused by Mutations in Rhodopsin

Retinitis pigmentosa (RP) is the most common group of inherited retinal degenerations and pathogenic variants in the Rhodopsin (RHO) gene are major cause for autosomal dominant RP (adRP). Despite extensive attempts to treat RHO-associated adRP, standardized curative treatment is still lacking. Recen...

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Detalles Bibliográficos
Autores principales: Kaukonen, Maria, McClements, Michelle E., MacLaren, Robert E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9330713/
https://www.ncbi.nlm.nih.gov/pubmed/35893064
http://dx.doi.org/10.3390/genes13081327

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9330713/
https://www.ncbi.nlm.nih.gov/pubmed/35893064
http://dx.doi.org/10.3390/genes13081327

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