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Article

Identification of mutations in members of the connexin gene family as a cause of nonsyndromic deafness in Taiwan.

Audiology & neuro-otology - 1 Jan 2007

Yang Jiann-Jou, Huang Shih-Hsin, Chou Kvei-Hsiu, Liao Pei-Ju, Su Ching-Chyuan, Li Shuan-Yow

Abstract excerpt

Connexins (Cx), a large family of membrane proteins, are key components of gap junction channels. These channels are critical intercellular pathways through which ions or small molecules are passed, regulating a variety of physiological and developmental processes. One of these processes is heari...

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Source

Identifiers

PMID: 17259707
DOI: 10.1159/000099024

Genes

GJA1
GJB1
GJB2
GJB3
GJB4
GJB6
GJE1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-17259707-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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