Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia.

Familial hemiplegic migraine (HM) is an autosomal dominant migraine with aura. In 20% of HM families, HM is associated with a mild permanent cerebellar ataxia (PCA). The CACNA1A gene encoding the alpha1A subunit of P/Q-type voltage-gated calcium channels is involved in 50% of unselected HM families...

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Autori principali: 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
Natura: Artigo
Lingua:Inglês
Pubblicazione: 1999
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Research Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC1377706/
https://ncbi.nlm.nih.gov/pubmed/9915947
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