Structural and mutational analysis of KCNQ2, the major gene locus for benign familial neonatal convulsions

Familial Hemiplegic Migraine and Episodic Ataxia Type-2 Are Caused by Mutations in the Ca2+ Channel Gene CACNL1A4

Roel A. Ophoff, Gisela M. Terwindt, Monique N. Vergouwe et al. · Cell · 1996 · 2.3K citations · Full text

Life Sciences, Neurology, Neuroscience +16

Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

Q. Wang, Mark Curran, Igor Splawski et al. · Nature Genetics · 1996 · 1.8K citations

Medicine, Genetics, Molecular Genetics +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 missense mutation in the neuronal nicotinic acetylcholine receptor α4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy

Ortrud K. Steinlein, John C. Mulley, Peter Propping et al. · Nature Genetics · 1995 · 1.1K citations

Life Sciences, Neurology, Neuroscience +12

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