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This gene encodes a protein involved intracellular vesicle and organelle transport, especially in the hair cell of the inner ear. Mutations in this gene have been found in patients with non-syndromic autosomal dominant and recessive hearing loss.
BC029719; DFNA22; DFNB37; KIAA0389; MYO6; myosin; myosin VI; myosin-VI; RGD1560646; Snell's waltzer; sv; tailchaser; Tlc; unconventional myosin; unconventional myosin-6; Unconventional myosin-VI
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