No abstract available
Publication types
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Letter
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Research Support, Non-U.S. Gov't
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Comment
MeSH terms
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Ataxia
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Databases, Genetic
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Humans
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Kv1.2 Potassium Channel
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Mutation
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Spastic Paraplegia, Hereditary*
Substances
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KCNA2 protein, human
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Kv1.2 Potassium Channel