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Article

[Analysis of positive rate of common genetic mutations in 1448 cases with different hearing phenotype].

Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery - 1 May 2011

Wang Guojian, Yuan Yongyi, Li Rong, Han Mingyu, Huang Shasha, Kang Dongyang, Zhang Xin, Dong Min, Dai Pu, Han Dongyi

Abstract excerpt

OBJECTIVE: To analyze the positive rate of common genetic mutations in Chinese non-syndromic sensorineural hearing loss groups with different hearing phenotype. METHOD: One thousand four hundred and forty-eight subjects with hearing test results received at least one of three genetic testings including: mutations in coding region of GJB2 and SLC26A4 with sequencing analysis and mitochondrial DNA C1494T/A1555G...

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Source

Identifiers

PMID: 21809555

Genes

GJB2

Variants

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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