ATP1A2 and benign familial infantile epilepsy: Other pathologies associated with ATP1A2 mutations were sensorineural hearing loss (V191M, Oh et al., 2015), basilar migraine (R548H, Ambrosini et al., 2005), benign familial infantile convulsions (BFIC; R689Q, Vanmolkot et al., 2003), generalized epilepsy with febrile seizures (GEFS+; G874S, Costa et al., 2014), pulmonary arterial hypertension (S940L, Montani et al., 2013) and reversible cerebral vasoconstriction (P979L Hermann et al., 2013).