Abstract
Identification of genes involved in hereditary vestibular disease is growing at a remarkable pace. Mutant mouse technology can be an important tool for understanding the biological mechanism of human vestibular diseases.
MeSH terms
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Animals
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Dyneins
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Eye Movements
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Humans
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Immunohistochemistry
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Mice
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Mice, Mutant Strains
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Myosin VIIa
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Myosins / metabolism
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Potassium Channels / genetics
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Potassium Channels / physiology
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Reflex, Vestibulo-Ocular
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Shaker Superfamily of Potassium Channels
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Vestibular Diseases / genetics*
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Vestibular Diseases / metabolism
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Vestibular Diseases / physiopathology
Substances
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MYO7A protein, human
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Myo7a protein, mouse
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Myosin VIIa
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Potassium Channels
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Shaker Superfamily of Potassium Channels
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Myosins
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Dyneins