Dual-vector gene therapy restores cochlear amplification and auditory sensitivity in a mouse model of DFNB16 hearing loss-Reference-Cited by-同舟云学术

Dual-vector gene therapy restores cochlear amplification and auditory sensitivity in a mouse model of DFNB16 hearing loss

Author:

Shubina-Oleinik Olga¹^ORCID,Nist-Lund Carl¹^ORCID,French Courtney²^ORCID,Rockowitz Shira²^ORCID,Shearer A. Eliot¹²,Holt Jeffrey R.¹³^ORCID

Affiliation:

1. Department of Otolaryngology, Boston Children’s Hospital and Harvard Medical School, Boston, MA 02115, USA.

2. Children’s Rare Disease Cohort Initiative, Boston Children’s Hospital, Boston, MA 02115, USA.

3. Department of Neurology, Boston Children’s Hospital and Harvard Medical School, Boston, MA 02115, USA.

Abstract

Dual-AAV delivery to outer hair cells restores hearing in a mouse model of DFNB16, a common form of genetic hearing loss.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference22 articles.

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