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Article

[Genotype and clinical phenotype analysis of 42 patients with delayed nonsyndromic hearing loss].

Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery - 1 Feb 2021

Niu Wenxia, Xu Huijuan, Qin Litao, Wang Guangke, Ding Shaoguang, Xie Cuncun, Jia Xiaodong, Liu Hongjian

Abstract excerpt

Objective:The aim of this study is to analyze the mutation characteristics of GJB2 and SLC26A4 gene in patients with delayed non-syndromic hearing loss, which is beneficial to the early detection and intervention of delayed deafness. Methods:Sanger sequencing technology was used to detect two common genes in 139 patients with non-syndromic deafness, six hot spot mutations in GJB2 gene and SLC26A4 gene, and single...

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Identifiers

PMID: 33540994
DOI: 10.13201/j.issn.2096-7993.2021.02.009
PMCID: PMC10127873

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