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Myoclonus epilepsy and ataxia due to KCNC1 mutation: Analysis of 20 cases and K+ channel properties

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To comprehensively describe the new syndrome of myoclonus epilepsy and ataxia due to potassium channel mutation (MEAK), including cellular electrophysiological characterization of observed clinical improvement with fever. Click to show full abstract

To comprehensively describe the new syndrome of myoclonus epilepsy and ataxia due to potassium channel mutation (MEAK), including cellular electrophysiological characterization of observed clinical improvement with fever.

Keywords: ataxia due; myoclonus epilepsy; kcnc1 mutation; epilepsy ataxia; due kcnc1

Journal Title: Annals of Neurology
Year Published: 2017

Link to full text (if available)


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