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Article

[Mutations in the connexin 26 gene in patients with nonsyndromic hearing impairment].

Zhonghua er bi yan hou ke za zhi - 1 Jun 2000

Xiao Z, Feng Y, Pan Q, Xie D, Shi X, Xia J

Abstract excerpt

OBJECTIVE: To determine the prevalence and characteristics of deafness-causing mutations in Connexin 26(Cx26, GJB2) gene in Chinese with nonsyndromic hearing impairment(NSHI). METHODS: Study subjects are all Chinese including 16 infants with sporadic congenital deaf-mutism, 39 patients with autosomal recessive hereditary hearing loss, 30 patients with autosomal dominant hereditary hearing loss and 100 normal...

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Identifiers

PMID: 12768774

Genes

GJB2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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