Adeno-Associated Viral Vectors as a Tool for Large Gene Delivery to the Retina

Gene therapy using adeno-associated viral (AAV) vectors currently represents the most promising approach for the treatment of many inherited retinal diseases (IRDs), given AAV’s ability to efficiently deliver therapeutic genes to both photoreceptors and retinal pigment epithelium, and their excellen...

Descripción completa

Detalles Bibliográficos
Autor principal: Trapani, Ivana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6523333/
https://www.ncbi.nlm.nih.gov/pubmed/30970639
http://dx.doi.org/10.3390/genes10040287

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6523333/
https://www.ncbi.nlm.nih.gov/pubmed/30970639
http://dx.doi.org/10.3390/genes10040287

Ejemplares similares