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Article

Prevalence and Clinical Characteristics of Hearing Loss Caused by MYH14 Variants.

Genes - 15 Oct 2021

Hiramatsu Ken, Nishio Shin-Ya, Kitajiri Shin-Ichiro, Kitano Tomohiro, Moteki Hideaki, Usami Shin-Ichi, On Behalf Of The Deafness Gene Study Consortium

Abstract excerpt

Variants in MYH14 are reported to cause autosomal dominant nonsyndromic hereditary hearing loss (ADNSHL), with 34 variants reported to cause hearing loss in various ethnic groups. However, the available information on prevalence, as well as with regard to clinical features, remains fragmentary. In this study, genetic screening for MYH14 variants was carried out using a large series of Japanese hearing-loss...

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Identifiers

PMID: 34681017
DOI: 10.3390/genes12101623
PMCID: PMC8535940

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