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

ABSTRACT: 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 patients to reveal more detailed information. Massively parallel DNA sequencing of 68 target candidate genes was applied in 8074 unrelated Japanese hearing-loss patients (including 1336 with ADNSHL) to identify genomic variations responsible for hearing loss. We identified 11 families with 10 variants. The prevalence was found to be 0.14% (11/8074) among all hearing-loss pa

SUBMITTER: Hiramatsu K 

PROVIDER: S-EPMC8535940 | biostudies-literature | 2021 Oct

REPOSITORIES: biostudies-literature