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2. Early onset, non fluctuating spinocerebellar ataxia and a novel missense mutation in CACNA1A gene. Tonelli A; D'Angelo MG; Salati R; Villa L; Germinasi C; Frattini T; Meola G; Turconi AC; Bresolin N; Bassi MT J Neurol Sci; 2006 Feb; 241(1-2):13-7. PubMed ID: 16325861 [TBL] [Abstract][Full Text] [Related]
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12. The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel. Ducros A; Denier C; Joutel A; Cecillon M; Lescoat C; Vahedi K; Darcel F; Vicaut E; Bousser MG; Tournier-Lasserve E N Engl J Med; 2001 Jul; 345(1):17-24. PubMed ID: 11439943 [TBL] [Abstract][Full Text] [Related]
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17. Identification of novel and recurrent CACNA1A gene mutations in fifteen patients with episodic ataxia type 2. Mantuano E; Romano S; Veneziano L; Gellera C; Castellotti B; Caimi S; Testa D; Estienne M; Zorzi G; Bugiani M; Rajabally YA; Barcina MJ; Servidei S; Panico A; Frontali M; Mariotti C J Neurol Sci; 2010 Apr; 291(1-2):30-6. PubMed ID: 20129625 [TBL] [Abstract][Full Text] [Related]
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