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Article

Research Progress of MYO6 Variant-Associated Hereditary Hearing Loss.

The journal of international advanced otology - 29 Apr 2026

Wu Zhijing, Bian Panpan, Xu Baicheng

Abstract excerpt

UNLABELLED: Hearing loss (HL) is the most common sensory disorder, with genetic factors accounting for approximately 60% of cases of congenital HL. Hearing loss is the most common sensory disorder, affecting approximately 60% of cases, which is often related to hereditary patterns. The MYO6 gene encodes the unconventional myosin VI, a protein crucial for maintaining the function of inner ear hair cells and the...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 42345434
DOI: 10.65717/iao.2026.252391

Genes

MYO6

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

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Research trail→

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Research Progress of MYO6 Variant-Associated Hereditary Hearing Loss.PMID 42345434Read ↗

Clinical Characteristics and In Vitro Analysis of MYO6 Variants Causing Late-Onset Progressive Hearing Loss.Semantic proximity Read ↗

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Mutations of MYO6 are associated with recessive deafness, DFNB37.Semantic proximity Read ↗

A novel MYO6 splice site mutation causes autosomal dominant sensorineural hearing loss type DFNA22 with a favourable outcome after cochlear implantation.Semantic proximity Read ↗

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Next-generation sequencing identifies three novel missense variants in ILDR1 and MYO6 genes in an Iranian family with hearing loss with review of the literature.Semantic proximity Read ↗

MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing loss.Semantic proximity Read ↗

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