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Article

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness.

Nature - 1 May 1997

Kelsell D P, Dunlop J, Stevens H P, Lench N J, Liang J N, Parry G, Mueller R F, Leigh I M

Abstract excerpt

Severe deafness or hearing impairment is the most prevalent inherited sensory disorder, affecting about 1 in 1,000 children. Most deafness results from peripheral auditory defects that occur as a consequence of either conductive (outer or middle ear) or sensorineuronal (cochlea) abnormalities. Although a number of mutant genes have been identified that are responsible for syndromic (multiple phenotypic disease)...

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Identifiers

PMID: 9139825
DOI: 10.1038/387080a0

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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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