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Article

Identification of a MYO7A mutation in a large Chinese DFNA11 family and genotype-phenotype review for DFNA11.

Acta oto-laryngologica - 1 May 2018

Li Lina, Yuan Hu, Wang Hongyang, Guan Jing, Lan Lan, Wang Dayong, Zong Liang, Liu Qiong, Han Bing, Huang Deliang, Wang Qiuju

Abstract excerpt

BACKGROUND: The molecular and genetic research showed the association between DFNA11 and mutations in MYO7A. This research aimed to identify a MYO7A mutation in a family with nonsyndromic autosomal dominant hearing loss. METHODS: We have ascertained one large multigenerational Chinese family (Z029) with autosomal dominant late-onset progressive non-syndromic sensorineural hearing loss. Genome-wide linkage...

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PMID: 29400105
DOI: 10.1080/00016489.2017.1397743

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

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