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Article

Government-funded universal newborn hearing screening and genetic analyses of deafness predisposing genes in Taiwan.

International journal of pediatric otorhinolaryngology - 1 Apr 2015

Chu Chun-Wei, Chen Yann-Jang, Lee Yi-Hui, Jaung Sian-Jang, Lee Fei-Peng, Huang Hung-Meng

Abstract excerpt

OBJECTIVE: To investigate the association of eight connexin genes (GJB2, GJB4, GJA1P1, GJB6, GJB3, GJA1, GJB1, and GJC3) and the SLC26A4 gene with congenital hearing impairment among infants in a universal newborn hearing screening program. METHOD: From September 2009 to October 2013, the consecutive neonates born in all six branches of Taipei City Hospital were enrolled. Infants who failed the newborn hearing...

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Source

Identifiers

PMID: 25724631
DOI: 10.1016/j.ijporl.2015.01.033

Genes

GJA1
GJB2
GJB3
GJB4
GJB1
GJB6
GJC3

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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