Recurrence of the T666M Calcium Channel CACNA1A Gene Mutation in Familial Hemiplegic Migraine with Progressive Cerebellar Ataxia-Reference-Cited by-同舟云学术

Recurrence of the T666M Calcium Channel CACNA1A Gene Mutation in Familial Hemiplegic Migraine with Progressive Cerebellar Ataxia

Published:1999-01 Issue:1 Volume:64 Page:89-98
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

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.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

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4. Familial hemiplegic migraine, nystagmus, and cerebellar atrophy;Elliott;Ann Neurol,1996

5. Migraine coma: meningitic migraine with cerebral oedema associated with a new form of autosomal dominant cerebellar ataxia;Fitzsimons;Brain,1985

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