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Article

A large cohort study of GJB2 mutations in Japanese hearing loss patients.

Clinical genetics - 1 Nov 2010

Tsukada K, Nishio S, Usami S

Abstract excerpt

GJB2 is the gene most frequently associated with hereditary hearing loss, and the GJB2 mutation spectrums vary among different ethnic groups. In this study, the mutation spectrum as well as clinical features of patients with GJB2 mutations as found in more than 1000 Japanese hearing loss families are summarized. The present results show that the frequency of GJB2 mutations in the Japanese population with hearing...

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Source

Identifiers

PMID: 20497192
DOI: 10.1111/j.1399-0004.2010.01407.x

Genes

GJB2

Provenance

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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