![Hypokalaemic periodic paralysis due to a novel ATP1A2 mutation: a new periodic paralysis gene?]()
Hypokalaemic periodic paralysis due to a novel ATP1A2 mutation: a new periodic paralysis gene?Matthews, E.; Zanoteli, E.; Scalco, R.S.; O’Callaghan, B.; Sud, R.; McCall, S.; Hanna, M.G.; Sampedro Castenada, M.; Männikkö, R.; Poulson, H. · Neuromuscular Disorders · 2017