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Article

A rapid method for simultaneous multi-gene mutation screening in children with nonsyndromic hearing loss.

Genomics - 1 Oct 2014

Du Wan, Cheng Jing, Ding Hui, Jiang Zhengwen, Guo Yufen, Yuan Huijun

Abstract excerpt

Hearing loss (HL) is a common genetically heterogeneous sensory disorder, occurring in 1 to 3 per 1000 live births. In spite of the extraordinary genetic heterogeneity, variants in GJB2, MT-RNR1, and SLC26A4 genes have been considered as the main reasons of nonsyndromic hearing loss in Chinese population. We developed a rapid multiplex genetic screening system called the SNPscan assay technique which could detect...

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Identifiers

PMID: 25149764
DOI: 10.1016/j.ygeno.2014.07.009

Genes

GJB2

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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