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Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia.
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.
Affiliation
  • Ducros A; Institut National de la Santé et de la Recherche Médicale (INSERM) U25, Faculté de Médecine Necker, 75730 Paris Cedex 15, France. tournier@necker.fr.
Am J Hum Genet ; 64(1): 89-98, 1999 Jan.
Article in En | MEDLINE | ID: mdl-9915947
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Calcium Channels / Cerebellar Ataxia / Migraine Disorders / Mutation Limits: Female / Humans / Male Language: En Journal: Am J Hum Genet Year: 1999 Document type: Article Affiliation country: France Country of publication: United States
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Calcium Channels / Cerebellar Ataxia / Migraine Disorders / Mutation Limits: Female / Humans / Male Language: En Journal: Am J Hum Genet Year: 1999 Document type: Article Affiliation country: France Country of publication: United States