{"id":"doi:10.1038/nbt.3781","kind":"article","title":"A synthetic AAV vector enables safe and efficient gene transfer to the mammalian inner ear","authors":["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"],"author_count":11,"year":2017,"published":"2017-02-06","venue":"Nature Biotechnology","cited_by":328,"doi":"10.1038/nbt.3781","arxiv_id":null,"nct_id":null,"source_url":"https://doi.org/10.1038/nbt.3781","archive_url":"https://space-kitty.com/papers/doi:10.1038/nbt.3781","updated":null,"pmid":"28165475","pmcid":null,"openalex_id":"W2586762515","pdf_url":null,"abstract":null,"abstract_license":null,"license":null,"is_open_access":true,"retracted":false,"peer_reviewed":null,"categories":["Virus-based gene therapy research"],"details":null,"provenance":"openalex","attribution":"Metadata and citation counts: OpenAlex (CC0).","topics":[{"slug":"gene-cell-therapy","name":"Gene & Cell Therapy","domain_slug":"medicine"}],"cited_in_dossiers":[]}