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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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| Publicado en: | Methods Mol Biol |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
2019
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| Assuntos: | |
| Acceso en liña: | 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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