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SubILM Injection of AAV for Gene Delivery to the Retina
Adeno-associated virus (AAV) has emerged as the vector of choice for delivering genes to the retina. Indeed, the first gene therapy to receive FDA approval in the United States is an AAV-based treatment for the inherited retinal disease, Leber congenital amaurosis-2. Voretigene neparvovec (Luxturna™...
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| Опубликовано в: : | Methods Mol Biol |
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| Главные авторы: | , , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
2019
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6700748/ https://ncbi.nlm.nih.gov/pubmed/30783978 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/978-1-4939-9139-6_14 |
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