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. 2017 May 22;7:46827. doi: 10.1038/srep46827

Corrigendum: Cochlear gene therapy with ancestral AAV in adult mice: complete transduction of inner hair cells without cochlear dysfunction

Jun Suzuki, Ken Hashimoto, Ru Xiao, Luk H Vandenberghe, M Charles Liberman
PMCID: PMC5439157  PMID: 28530226

Scientific Reports 7: Article number: 45524 10.1038/srep45524; published online: April 03 2017; updated: May 22 2017

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:

“In order to maximize transduction efficiencies, a “designer” AAV vector, AAV2/Anc80L65, was tested based on promising results in organotypic explant cultures and in vivo studies in newborn mice1,2”.

References

  1. 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). [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. 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). [DOI] [PMC free article] [PubMed] [Google Scholar]

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