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 thei...
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| Format: | Article |
| Language: | English |
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MDPI AG
2019-04-01
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| Series: | Genes |
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| Online Access: | https://www.mdpi.com/2073-4425/10/4/287 |