A novel MYH14 mutation in a Chinese family with autosomal dominant nonsyndromic hearing loss | BMC Medical Genetics | Full Text

A novel MYH14 mutation in a Chinese family with autosomal dominant nonsyndromic hearing loss | BMC Medical Genetics | Full Text

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

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 deafnes...

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

Citation:BMC Medical Genetics 2020 21:154

Content type:Research article

 

Published on: 25 July 2020

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