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Article

Function and expression pattern of nonsyndromic deafness genes.

Current molecular medicine - 1 Jun 2009

Hilgert Nele, Smith Richard J H, Van Camp Guy

Abstract excerpt

Hearing loss is the most common sensory disorder, present in 1 of every 500 newborns. To date, 46 genes have been identified that cause nonsyndromic hearing loss, making it an extremely heterogeneous trait. This review provides a comprehensive overview of the inner ear function and expression pattern of these genes. In general, they are involved in hair bundle morphogenesis, form constituents of the extracellular...

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Identifiers

PMID: 19601806
DOI: 10.2174/156652409788488775
PMCID: PMC2840995

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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