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Article

[Mutations of GJB2 gene in infants with non-syndromic hearing impairment].

Zhonghua yi xue za zhi - 16 Mar 2005

Shi Gui-Zhi, Gong Lu-Xia, Nie Wen-Ying, Lin Qian, Xiang Li-Li, Xu Xiao-Hu, Qi Yi-Sheng

Abstract excerpt

OBJECTIVE: To explore the relationship between GJB2 gene mutations and severe-to-profound bilateral non-syndromic hearing impairment (NSHI). METHODS: Peripheral blood was collected from 20 infants with severe-to-profound bilateral NSHI confirmed by otoacoustic emissions (OAE), auditory brainstem responses (ABR) and clinical physical examination, 11 male and 9 female, aged 3 months to 3 years. PCR and sequencing...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 15932734

Genes

GJB2
ABR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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