No abstract available
MeSH terms
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Chromosomes, Human, Pair 20 / genetics
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Chromosomes, Human, Pair 8 / genetics
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Deafness / genetics*
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Deafness / physiopathology
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Disease Progression
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Epilepsy, Benign Neonatal / genetics*
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Epilepsy, Benign Neonatal / physiopathology
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Genes, Dominant
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Hair Cells, Auditory, Outer / physiopathology
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Humans
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Mutation
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Potassium Channels / genetics*
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Potassium Channels / physiology*