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

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

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Record

Archive ID
doi:10.1038/nbt.3781
Published
Feb 6, 2017
Venue
Nature Biotechnology
DOI
10.1038/nbt.3781
PubMed
28165475
Categories
Virus-based gene therapy research
Provenance
openalex

Topics