Epilepsy-causing mutations in Kv7.2 C-terminus affect binding and functional modulation by calmodulin

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Synaptic Transmission, Molecular Biology, Neurotransmission +17

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

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

Zongming Pan, Tingching Kao, Zsolt Horváth et al. · Journal of Neuroscience · 2006 · 570 citations · Full text

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

Sarah Weckhuysen, Simone Mandelstam, Arvid Suls et al. · Annals of Neurology · 2011 · 494 citations