Publication | Open Access

MYO6, the Human Homologue of the Gene Responsible for Deafness in Snell’s Waltzer Mice, Is Mutated in Autosomal Dominant Nonsyndromic Hearing Loss

Is MutatedDevelopmental BiologyMendelian DisorderGenetic DisorderGeneticsWaltzer MiceAuditory PhysiologyGene ResponsibleMolecular GeneticsAuditory ResearchArtsMedicineAuditory SystemHearing Loss