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References
Pan, B. et al. Gene therapy restores auditory and vestibular function in a mouse model of Usher syndrome type 1c. Nat. Biotechnol. 35, 264–272 (2017)
Landegger, L. D. et al. A synthetic AAV vector enables safe and efficient gene transfer to the mammalian inner ear. Nat. Biotechnol. 35, 280–284 (2017)
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Kingwell, K. Vector overcomes barrier to gene therapy delivery. Nat Rev Drug Discov 16, 238–239 (2017). https://doi.org/10.1038/nrd.2017.58
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DOI: https://doi.org/10.1038/nrd.2017.58