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Article

Nuclear and mitochondrial genes mutated in nonsyndromic impaired hearing.

International journal of pediatric otorhinolaryngology - 1 May 2005

Finsterer Josef, Fellinger Johannes

Abstract excerpt

Half of the cases with congenital impaired hearing are hereditary (HIH). HIH may occur as part of a multisystem disease (syndromic HIH) or as disorder restricted to the ear and vestibular system (nonsyndromic HIH). Since nonsyndromic HIH is almost exclusively caused by cochlear defects, affected patients suffer from sensorineural hearing loss. One percent of the total human genes, i.e. 300-500, are estimated to...

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Source

Identifiers

PMID: 15850684
DOI: 10.1016/j.ijporl.2004.12.002

Genes

GJB2
GJB6
TECTA
CDH23
DSPP
GJB3
KCNQ4
MYH9
MYO6
PCDH15
TMC1
WFS1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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