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Article

Forty-six genes causing nonsyndromic hearing impairment: which ones should be analyzed in DNA diagnostics?

Mutation research - 1 Jan 2000

Hilgert Nele, Smith Richard J H, Van Camp Guy

Abstract excerpt

Hearing impairment is the most common sensory disorder, present in 1 of every 500 newborns. With 46 genes implicated in nonsyndromic hearing loss, it is also an extremely heterogeneous trait. Here, we categorize for the first time all mutations reported in nonsyndromic deafness genes, both worldw...

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Identifiers

PMID: 18804553
DOI: 10.1016/j.mrrev.2008.08.002
PMCID: PMC2847850

Genes

GJB2
WFS1
CDH23
COCH
KCNQ4
OTOF
TMC1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-18804553-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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