Associated Papers
The Prevalence and Clinical Characteristics of MYO3A-Associated Hearing Loss in 15,684 Hearing Loss Patients.
Maekawa K et al.
Genes, 2025
Molecular insights into MYO3A kinase domain variants explain variability in both severity and progression of DFNB30 hearing impairment.
Souissi A et al.
Journal of Biomolecular Structure & Dynamics, 2022
A novel missense variant in MYO3A is associated with autosomal dominant high-frequency hearing loss in a German family.
Doll J et al.
Molecular Genetics & Genomic Medicine, 2020
Characterization of a novel MYO3A missense mutation associated with a dominant form of late onset hearing loss.
Dantas VGL et al.
Scientific Reports, 2018
Identification of a novel homozygous mutation in MYO3A in a Chinese family with DFNB30 non-syndromic hearing impairment.
Qu R et al.
International Journal of Pediatric Otorhinolaryngology, 2016
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