A recurrent KCNQ2 pore mutation causing early onset epileptic encephalopathy has a moderate effect on M current but alters subcellular localization of Kv7 channels

KCNQ2 and KCNQ3 Potassium Channel Subunits: Molecular Correlates of the M-Channel

H. Wang · 1998 · 1.3K citations

Life Sciences, Biophysics, Neuroscience +17

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

Nanda A. Singh, Carole Charlier, Dora Stauffer et al. · Nature Genetics · 1998 · 1.2K citations

Life Sciences, Genetics, Molecular Genetics +14

A Potassium Channel Mutation in Neonatal Human Epilepsy

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

Life Sciences, Genetics, Molecular Genetics +17

A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family

Carole Charlier, Nanda A. Singh, Stephen G. Ryan et al. · Nature Genetics · 1998 · 939 citations

Life Sciences, Genetics, Molecular Genetics +16

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 · 579 citations · Full text

Life Sciences, Neurobiology, Neuroscience +17