The authors forgot to cite previous studies relating to in vivo studies in newborn mice. These additional references are listed below as references 1 and 2, and should appear in the text as below.
In the Introduction section,
“In order to maximize transduction efficiencies, a “designer” AAV vector, AAV2/Anc80L65, was tested based on promising results in organotypic explant cultures”.
should read:
References
Landegger, L. D. et al. A Synthetic AAV vector enables safe and efficient gene transfer to the mammalian inner ear. Nat. Biotechnol. 35(3), 280–284, doi: 10.1038/nbt.3781 (2017).
Pan, B. et al. Gene therapy restores auditory and vestibular Function in a Mouse Model of Usher Syndrome Type 1c. Nat. Biotechnol. 35(3), 264–272, doi: 10.1038/nbt.3801 (2017).
Additional information
The online version of the original article can be found at 10.1038/srep45524
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Suzuki, J., Hashimoto, K., Xiao, R. et al. Correction: Corrigendum: Cochlear gene therapy with ancestral AAV in adult mice: complete transduction of inner hair cells without cochlear dysfunction. Sci Rep 7, 46827 (2017). https://doi.org/10.1038/srep46827
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DOI: https://doi.org/10.1038/srep46827
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