A novel ATP1A2 mutation in a patient with hypokalaemic periodic paralysis and CNS symptoms - Castaneda, Marisol Sampedro; Zanoteli, Edmar; Scalco, Renata S.; Scaramuzzi, Vinicius; Caldas, Vitor Marques; Reed, Umbertina Conti; Silva, Andre Macedo Serafim da; O'callaghan, Benjamin; Phadke, Rahul; Bugiardini, Enrico (Brain, 2018)