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

• मुख्य लेखकों: Mingming Wang (लेखक), Yicui Zhou (लेखक), Fengguo Zhang (लेखक), Zhaomin Fan (लेखक), Xiaohui Bai (लेखक), Haibo Wang (लेखक)
• स्वरूप: पुस्तक
• प्रकाशित: BMC, 2020-07-01T00:00:00Z.
• विषय: article
• ऑनलाइन पहुंच: Connect to this object online.

Abstract 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 H...