A novel ATP1A2 mutation in a...

Brain 2018 / 11

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

Sampedro Castañeda, Marisol, Zanoteli, Edmar, Scalco, Renata S, Scaramuzzi, Vinicius, Marques Caldas, Vitor, Conti Reed, Umbertina, da Silva, Andre Macedo Serafim, O’Callaghan, Benjamin, Phadke, Rahul
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Language:
english
Journal:
Brain
DOI:
10.1093/brain/awy283
Date:
November, 2018
File:
PDF, 1.49 MB
english, 2018
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