martes, 28 de julio de 2020

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

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
 
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