Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel

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

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

Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel ß1 subunit gene SCN1B

Robyn H. Wallace, Dao Wen Wang, Rita Singh et al. · Nature Genetics · 1998 · 1K citations

Life Sciences, Genetics, Neuroscience +14

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

Primary structure and functional expression from complementary DNA of a brain calcium channel

Yasuo Mori, Thomas Friedrich, Man-Suk Kim et al. · Nature · 1991 · 869 citations

Life Sciences, Molecular Biology, Neuroscience +17