A novel ATP1A2 mutation in a patient with hypokalaemic periodic paralysis and CNS symptoms

Sampedro Castañeda, M; Zanoteli, E; Scalco, RS; Scaramuzzi, V; Marques Caldas, V; Conti Reed, U; da Silva, AMS; ... Matthews, E; + view all Sampedro Castañeda, M; Zanoteli, E; Scalco, RS; Scaramuzzi, V; Marques Caldas, V; Conti Reed, U; da Silva, AMS; O'Callaghan, B; Phadke, R; Bugiardini, E; Sud, R; McCall, S; Hanna, MG; Poulsen, H; Männikkö, R; Matthews, E; - view fewer (2018) A novel ATP1A2 mutation in a patient with hypokalaemic periodic paralysis and CNS symptoms. Brain 10.1093/brain/awy283 . (In press). Green open access

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