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Article

The application of genome editing in studying hearing loss.

Hearing research - 1 Sept 2015

Zou Bing, Mittal Rahul, Grati M'hamed, Lu Zhongmin, Shu Yilai, Tao Yong, Feng Youg, Xie Dinghua, Kong Weijia, Yang Shiming, Chen Zheng-Yi, Liu Xuezhong

Abstract excerpt

Targeted genome editing mediated by clustered, regularly interspaced, short palindromic repeat (CRISPR)/CRISPR-associated nuclease 9 (Cas9) technology has emerged as one of the most powerful tools to study gene functions, and with potential to treat genetic disorders. Hearing loss is one of the most common sensory disorders, affecting approximately 1 in 500 newborns with no treatment. Mutations of inner ear genes...

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Share to Clustered Regularly Interspaced Short Palindromic Repeats
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 25987504
DOI: 10.1016/j.heares.2015.04.016
PMCID: PMC4554948

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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