# A synthetic AAV vector enables safe and efficient gene transfer to the mammalian inner ear

Article · Lukas David Landegger, Bifeng Pan, Charles Askew, Sarah Wassmer, Sarah D Gluck, Alice Galvin, Ruth Taylor, Andrew Forge, Konstantina M. Stanković, Jeffrey R. Holt, Luk H. Vandenberghe

- Archive id: doi:10.1038/nbt.3781
- Published: 2017-02-06
- Venue: Nature Biotechnology
- DOI: https://doi.org/10.1038/nbt.3781
- PMID: 28165475
- Citations: 328
- Source URL: https://doi.org/10.1038/nbt.3781
- Provenance: openalex

_Abstract not reproduced: its license does not permit redistribution. See the source URL._

Topics: [Gene & Cell Therapy](https://space-kitty.com/topics/gene-cell-therapy)

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