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
- 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]
- 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]