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Article

Gene localization in a Chinese family with autosomal dominant non-syndromic deafness.

Acta oto-laryngologica - 1 Oct 2011

Jiang Lu, Liu Yalan, Feng Yong, Hu Zhengmao, Mei Lingyun, Long Liwei, Chen Hongsheng, Xue Jingjie, Xia Kun, He Chufeng

Abstract excerpt

CONCLUSIONS: There could be another candidate gene in DFNA2, which could be responsible for the hearing loss phenotype. OBJECTIVE: We collected a four-generation family from the southern part of China with autosomal dominant sensorineural hearing impairment. In order to identify the responsible pathogenic mutations in this family, we set out to identify the locus and to sequentially analyze the candidate genes in...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 21651318
DOI: 10.3109/00016489.2011.591822

Genes

GJB3
KCNQ4

Provenance

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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