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AAV2.7m8 is a powerful viral vector for inner ear gene therapy
Adeno-associated virus (AAV) has been successfully used to deliver gene therapy to improve auditory function in mouse models of hereditary hearing loss. Many forms of hereditary hearing loss have mutations which affect the cochlear hair cells, the mechanosensory cells which allow for sound detection...
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| Publié dans: | Nat Commun |
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| Auteurs principaux: | , , , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
Nature Publishing Group UK
2019
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6347594/ https://ncbi.nlm.nih.gov/pubmed/30683875 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41467-018-08243-1 |
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