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2. Congenital ataxia and hemiplegic migraine with cerebral edema associated with a novel gain of function mutation in the calcium channel CACNA1A. García Segarra N; Gautschi I; Mittaz-Crettol L; Kallay Zetchi C; Al-Qusairi L; Van Bemmelen MX; Maeder P; Bonafé L; Schild L; Roulet-Perez E J Neurol Sci; 2014 Jul; 342(1-2):69-78. PubMed ID: 24836863 [TBL] [Abstract][Full Text] [Related]
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8. Two distinct phenotypes, hemiplegic migraine and episodic Ataxia type 2, caused by a novel common CACNA1A variant. Nardello R; Plicato G; Mangano GD; Gennaro E; Mangano S; Brighina F; Raieli V; Fontana A BMC Neurol; 2020 Apr; 20(1):155. PubMed ID: 32336275 [TBL] [Abstract][Full Text] [Related]
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13. CACNA1A-p.Thr501Met mutation associated with familial hemiplegic migraine: a family report. Romozzi M; Primiano G; Rollo E; Travaglini L; Calabresi P; Servidei S; Vollono C J Headache Pain; 2021 Jul; 22(1):85. PubMed ID: 34320921 [TBL] [Abstract][Full Text] [Related]
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