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A novel KCNA1 mutation identified in an Italian family affected by episodic ataxia type 1. by Imbrici, P, Gualandi, F, D'Adamo, M, Masieri, M, Cudia, P, De Grandis, D, Mannucci, R, Nicoletti, I, Tucker, S, Ferlini, A, Pessia, M
Published 2008Journal article