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- W2040456165 abstract "Abstract Episodic ataxia and myokymia syndrome is an autosomal dominant disorder characterized by persistent myokymia and attacks of unsteadiness, slurred speech, and tremulousness. This disease has been associated with point mutations in the potassium channel gene Kv1.1 (KCNA1), located at chromosome 12p13. Here, we describe a novel mutation within this gene in a newly diagnosed family." @default.
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- W2040456165 title "Episodic ataxia and myokymia syndrome: A new mutation of potassium channel gene Kv1.1" @default.
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- W2040456165 doi "https://doi.org/10.1002/ana.410400422" @default.
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