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Article

Mouse otocyst transuterine gene transfer restores hearing in mice with connexin 30 deletion-associated hearing loss.

Molecular therapy : the journal of the American Society of Gene Therapy - 1 Jun 2013

Miwa Toru, Minoda Ryosei, Ise Momoko, Yamada Takao, Yumoto Eiji

Abstract excerpt

Although numerous causative genes for hereditary hearing loss have been identified, there are no fundamental treatments for this condition. Herein, we describe a novel potential treatment for genetic hearing loss. Because mutations or deletions in the connexin (Cx) genes are common causes of profound congenital hearing loss in both humans and mice, we investigated whether gene supplementation therapy using the...

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Identifiers

PMID: 23587925
DOI: 10.1038/mt.2013.62
PMCID: PMC3677317

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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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Mouse otocyst transuterine gene transfer restores hearing in mice with connexin 30 deletion-associated hearing loss.PMID 23587925Read ↗

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