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Article

[Mutation analysis of 16 mutation spots related to children patients with non-syndromic sensorineural hearing loss].

Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery - 1 Feb 2015

Man Rongjun, Zhang Zeng, Lu Rongzhong, Wang Xiao, Sun Shiping, Wang Dan, Xu Xiaosong, Wang Weiguo, Wang Huizhong

Abstract excerpt

OBJECTIVE: To explore the clinical signification of screening 16 target deafness mutations in GJB2, GJB3, SLC26A4, WFS1 and mitochondrial DNA 12S rRNA in 135 children patients with non-syndromic sensorineural hearing loss (NSHL) in Zibo City, Shandong province. METHOD: Peripheral blood samples of 135 subjects in the study diagnosed as NSHL were collected; Polymerase chain reaction (PCR) and direct sequencing were...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to DNA, Mitochondrial

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Source

Identifiers

PMID: 26121829

Genes

GJB2
WFS1
GJB3

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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