Adeno-Associated Viral Vectors as a Tool for Large Gene Delivery to the Retina
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DOI: 10.3390/genes10040287
Abstract: 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… read more here.
Keywords: viral vectors; vectors tool; associated viral; aav vectors ... See more keywords