No abstract available
Keywords:
etiology: genetic disorder; localization: not applicable; phenomenology: not applicable; syndrome: not applicable.
MeSH terms
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Adult
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Ataxia / genetics
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Epilepsy* / genetics
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Humans
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Kv1.2 Potassium Channel / genetics
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Mutation
Substances
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KCNA2 protein, human
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Kv1.2 Potassium Channel