Abstract
The complexity of genetic pathways for hearing is beginning to be amenable to unraveling by systematic functional genomic analysis. Genome-wide mutagenesis studies in the mouse are beginning to shed further light on the structure and regulation of the machinery of hearing.
MeSH terms
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Animals
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Deafness / genetics
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Disease Models, Animal
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Genetic Markers / genetics
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Genetic Markers / physiology
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Hearing / genetics*
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Humans
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Mutagenesis, Site-Directed / genetics
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Mutagenesis, Site-Directed / physiology
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Organ of Corti / pathology
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Organ of Corti / physiology
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Postural Balance / physiology
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Sensation Disorders / genetics
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Signal Transduction / genetics
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Signal Transduction / physiology