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Article

Genetic association of MYH genes with hereditary hearing loss in Korea.

Gene - 10 Oct 2016

Kim Sang-Joo, Lee Seokwon, Park Hong-Joon, Kang Tae-Hun, Sagong Borum, Baek Jeong-In, Oh Se-Kyung, Choi Jae Young, Lee Kyu-Yup, Kim Un-Kyung

Abstract excerpt

BACKGROUND: Myosin is a key protein involved in regulating the shape and motility of cells. The MYH9 and MYH14 genes, which encode non-muscle myosin heavy chain IIA (NMMHC II-A) and IIC (NMMHC II-C), respectively, are expressed in the inner ear. These myosin genes are known to be associated with autosomal dominant non-syndromic hearing loss (ADNSHL); however, genetic studies in patients with ADNSHL in Korea have...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 27393652
DOI: 10.1016/j.gene.2016.07.011

Genes

MYH14
MYH9

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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