Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia
家族性偏瘫性偏头痛伴进行性小脑共济失调中T666M钙通道CACNA1A基因突变的复发
期刊:American Journal of Human Genetics
影响因子:8.1
doi:10.1086/302192
Ducros, A; Denier, C; Joutel, A; Vahedi, K; Michel, A; Darcel, F; Madigand, M; Guerouaou, D; Tison, F; Julien, J; Hirsch, E; Chedru, F; Bisgård, C; Lucotte, G; Després, P; Billard, C; Barthez, M A; Ponsot, G; Bousser, M G; Tournier-Lasserve, E
