Clinical characteristics of KCNQ2 encephalopathy

<scp>ILAE</scp> classification of the epilepsies: Position paper of the <scp>ILAE</scp> Commission for Classification and Terminology

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A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns

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A Potassium Channel Mutation in Neonatal Human Epilepsy

Christian Biervert, Björn C. Schroeder, Christian Kubisch et al. · Science · 1998 · 1.1K citations

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A Common Ankyrin-G-Based Mechanism Retains KCNQ and Na_VChannels at Electrically Active Domains of the Axon

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<i>KCNQ2</i> encephalopathy: Emerging phenotype of a neonatal epileptic encephalopathy

Sarah Weckhuysen, Simone Mandelstam, Arvid Suls et al. · Annals of Neurology · 2011 · 514 citations

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