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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...
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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MDPI
2019
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| 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 |