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Article

A novel MYH14 mutation in a Chinese family with autosomal dominant nonsyndromic hearing loss.

BMC medical genetics - 25 Jul 2020

Wang Mingming, Zhou Yicui, Zhang Fengguo, Fan Zhaomin, Bai Xiaohui, Wang Haibo

Abstract excerpt

BACKGROUND: MYH14 gene mutations have been suggested to be associated with nonsyndromic/syndromic sensorineural hearing loss. It has been reported that mutations in MYH14 can result in autosomal dominant nonsyndromic deafness-4A (DFNA4). METHODS: In this study, we examined a four-generation Han Chinese family with nonsyndromic hearing loss. Targeted next-generation sequencing of deafness genes was employed to...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 32711451
DOI: 10.1186/s12881-020-01086-y
PMCID: PMC7382048

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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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