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Article

Molecular genetics applied to clinical practice: the Cx26 hearing impairment.

British journal of audiology - 1 Oct 1999

Orzan E, Polli R, Martella M, Vinanzi C, Leonardi M, Murgia A

Abstract excerpt

Mutations in the Cx26/GJB2 gene account for a large proportion of pre-lingual hearing impairment with a prevalence up to 50% in autosomal recessive cases and a still undefined prevalence in sporadic cases. Ninety-four subjects affected by non-syndromal sensorineural hearing impairment (NSHI) were enrolled in the study. The patients had either a family history of childhood hearing deficit or represented sporadic...

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Source

Identifiers

PMID: 10890143
DOI: 10.3109/03005369909090112

Genes

GJB2

Provenance

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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