Gene editing based hearing impairment research and therapeutics.

Abstract:

:Hearing impairment affects 1 in 500 newborns worldwide and nearly one out of three people over the age of 65 (WHO, 2019). Hereditary hearing loss is the most common type of congenital deafness; genetic factors also affect deafness susceptibility. Gene therapies may preserve or restore natural sound perception, and have rescued deafness in multiple hereditary murine models. CRISPR-Cas9 and base editors (BEs) are newly developed gene editing technologies that can facilitate gene studies in the inner ear and provide therapeutic approaches for hearing impairment. Here, we present recent applications of gene editing in the inner ear.

journal_name

Neurosci Lett

journal_title

Neuroscience letters

authors

Kang W,Sun Z,Zhao X,Wang X,Tao Y,Wu H

doi

10.1016/j.neulet.2019.134326

subject

Has Abstract

pub_date

2019-09-14 00:00:00

pages

134326

eissn

0304-3940

issn

1872-7972

pii

S0304-3940(19)30425-2

journal_volume

709

pub_type

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