Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the P/Q-type calcium channel alfa 1-subunit gene (CACNL1A4) on chromosome 19p13.1

OPHOFF R.A.;TERWINDT G.M.;VERGOUWEL M.N.;VAN EIJK R.;OEFNER P.J.;HOFFMAN S.M.G.;LAMERDIN J.E.;MOHRENWEISER H.W.;BULMAN D.E.;FERRARI , MAURIZIO;HAAN J.;FRANTS R.R.

1996-01-01