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47. Migraine, ataxia and epilepsy: a challenging spectrum of genetically determined calcium channelopathies. Dutch Migraine Genetics Research Group. Terwindt GM; Ophoff RA; Haan J; Sandkuijl LA; Frants RR; Ferrari MD Eur J Hum Genet; 1998; 6(4):297-307. PubMed ID: 9781035 [TBL] [Abstract][Full Text] [Related]
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49. Familial hemiplegic migraine type 2 is linked to 0.9Mb region on chromosome 1q23. Marconi R; De Fusco M; Aridon P; Plewnia K; Rossi M; Carapelli S; Ballabio A; Morgante L; Musolino R; Epifanio A; Micieli G; De Michele G; Casari G Ann Neurol; 2003 Mar; 53(3):376-81. PubMed ID: 12601705 [TBL] [Abstract][Full Text] [Related]
50. Expanding the phenotypic spectrum of the CACNA1A gene T666M mutation: a description of 5 families with familial hemiplegic migraine. Kors EE; Haan J; Giffin NJ; Pazdera L; Schnittger C; Lennox GG; Terwindt GM; Vermeulen FL; Van den Maagdenberg AM; Frants RR; Ferrari MD Arch Neurol; 2003 May; 60(5):684-8. PubMed ID: 12756131 [TBL] [Abstract][Full Text] [Related]
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