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

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...

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Main Authors: Mingming Wang (Author), Yicui Zhou (Author), Fengguo Zhang (Author), Zhaomin Fan (Author), Xiaohui Bai (Author), Haibo Wang (Author)
Format: Book
Published: BMC, 2020-07-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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