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...

Source: BMC Medical Genetics - July 25, 2020 Category: Genetics & Stem Cells Authors: Mingming Wang, Yicui Zhou, Fengguo Zhang, Zhaomin Fan, Xiaohui Bai and Haibo Wang Tags: Research article Source Type: research