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Article

Multiplex detection of common mutations in the Connexin-26 gene.

Genetic testing - 1 Jan 2003

Baris I, Köksal V

Abstract excerpt

Hearing impairment that results from inherited genetic defects occurs in approximately 1/2,000 live births. Mutations in the Connexin-26 gene have been shown to be a major contributor to prelingual, nonsyndromic, autosomal recessive deafness in many populations. The most common mutations in this...

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PMID: 12820705
DOI: 10.1089/109065703321560967

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-12820705-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

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Multiplex detection of common mutations in the Connexin-26 gene.PMID 12820705Read ↗

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Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss.Semantic proximity Read ↗

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