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Downbeat Nystagmus in Episodic Ataxia Type 1 Associated with a Novel KCNA1 Mutation

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Ataxia / complications Ataxia / genetics Humans Kv1.1 Potassium Channel / genetics Mutation / genetics Myokymia* Nystagmus, Pathologic* / genetics HSAC NEU

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Mov Disord . 2022 Feb;37(2):430-432

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Wiley

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