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Article

Molecular etiology of hearing impairment in Inner Mongolia: mutations in SLC26A4 gene and relevant phenotype analysis.

Journal of translational medicine - 30 Nov 2008

Dai Pu, Yuan Yongyi, Huang Deliang, Zhu Xiuhui, Yu Fei, Kang Dongyang, Yuan Huijun, Wu Bailin, Han Dongyi, Wong Lee-Jun C

Abstract excerpt

BACKGROUND: The molecular etiology of hearing impairment in Chinese has not been thoroughly investigated. Study of GJB2 gene revealed that 30.4% of the patients with hearing loss in Inner Mongolia carried GJB2 mutations. The SLC26A4 gene mutations and relevant phenotype are analyzed in this study. METHODS: One hundred and thirty-five deaf patients were included. The coding exons of SLC26A4 gene were sequence...

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Identifiers

PMID: 19040761
DOI: 10.1186/1479-5876-6-74
PMCID: PMC2630943

Genes

GJB2

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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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