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rAAV-Mediated Cochlear Gene Therapy: Prospects and Challenges for Clinical Application
Over the last decade, pioneering molecular gene therapy for inner-ear disorders have achieved experimental hearing improvements after a single local or systemic injection of adeno-associated, virus-derived vectors (rAAV for recombinant AAV) encoding an extra copy of a normal gene, or ribozymes used...
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| Publicat a: | J Clin Med |
|---|---|
| Autors principals: | , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
MDPI
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7073754/ https://ncbi.nlm.nih.gov/pubmed/32098144 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/jcm9020589 |
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