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Article

GJB2 gene mutations in newborns with non-syndromic hearing impairment in Northern China.

Hearing research - 1 Nov 2004

Shi Gui-zhi, Gong Lu-xia, Xu Xiao-hu, Nie Wen-ying, Lin Qian, Qi Yi-sheng

Abstract excerpt

Mutations in GJB2 account for the majority of recessive forms of prelingual hearing loss. However, in most previous studies it was not possible to distinguish between congenital (present at birth) and non-congenital prelingual hearing loss. In the present study, the frequency of GJB2 alleles in 20 newborns with bilateral severe-to-profound non-syndromic hearing impairment (NSHI) who were found at birth through...

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Source

Identifiers

PMID: 15504600
DOI: 10.1016/j.heares.2004.06.012

Genes

GJB2

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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