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, Ronald Van Eijk, Peter J. Oefner, Susan M G Hoffman, Jane E. Lamerdin, Harvey W. Mohrenweiser, Dennis E. Bulman, Maurizio Ferrari, Joost Haan, Dick Lindhout, Gert Jan B Van Ommen, Marten H. Hofker, Michel D. Ferrari, Rune R. Frants