Contribution of the central hydrophobic residue in the PXP motif of voltage-dependent K+ channels to S6 flexibility and gating properties. par Imbrici, P, Grottesi, A, D'Adamo, M, Mannucci, R, Tucker, S, Pessia, M

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