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AAV-ie enables safe and efficient gene transfer to inner ear cells
Hearing loss is the most common sensory disorder. While gene therapy has emerged as a promising treatment of inherited diseases like hearing loss, it is dependent on the identification of gene delivery vectors. Adeno-associated virus (AAV) vector-mediated gene therapy has been approved in the US for...
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| Vydáno v: | Nat Commun |
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| Hlavní autoři: | , , , , , , , , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Nature Publishing Group UK
2019
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6700137/ https://ncbi.nlm.nih.gov/pubmed/31427575 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41467-019-11687-8 |
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