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 MA, Ponsot G, Bousser MG, Tournier-Lasserve E.
Ducros A, et al. Among authors: bousser mg.
Am J Hum Genet. 1999 Jan;64(1):89-98. doi: 10.1086/302192.
Am J Hum Genet. 1999.
PMID: 9915947
Free PMC article.