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Article

GJB2 (connexin 26) mutations are not a major cause of hearing loss in the Indonesian population.

American journal of medical genetics. Part A - 1 Jun 2005

Snoeckx Rikkert L, Djelantik Bulantrisna, Van Laer Lut, Van de Heyning Paul, Van Camp Guy

Abstract excerpt

Although hereditary hearing loss is a very heterogeneous disorder, variants in one gene, GJB2 (connexin 26), account for up to 50% of autosomal recessive nonsyndromal sensorineural hearing loss in most populations. This study investigates the contribution of GJB2 to autosomal recessive nonsyndromal hearing loss in the Indonesian population. We performed DNA sequence analysis in 120 patients with profound early...

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Source

Identifiers

PMID: 15832357
DOI: 10.1002/ajmg.a.30726

Genes

GJB2

Variants

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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