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5. 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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10. Early-onset progressive ataxia associated with the first CACNA1A mutation identified within the I-II loop. Cricchi F; Di Lorenzo C; Grieco GS; Rengo C; Cardinale A; Racaniello M; Santorelli FM; Nappi G; Pierelli F; Casali C J Neurol Sci; 2007 Mar; 254(1-2):69-71. PubMed ID: 17292920 [TBL] [Abstract][Full Text] [Related]
11. Newly characterised 5' and 3' regions of CACNA1A gene harbour mutations associated with Familial Hemiplegic Migraine and Episodic Ataxia. Veneziano L; Guida S; Mantuano E; Bernard P; Tarantino P; Boccone L; Hisama FM; Carrera P; Jodice C; Frontali M J Neurol Sci; 2009 Jan; 276(1-2):31-7. PubMed ID: 18976783 [TBL] [Abstract][Full Text] [Related]
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20. Episodic ataxia type 2: an uncommon inherited CNS channelopathies. Pulkes T J Med Assoc Thai; 2003 Apr; 86(4):376-80. PubMed ID: 12757085 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]