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

Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaper › Journal article › Research › peer-review

Marisol Sampedro Castañeda, Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London
Edmar Zanoteli, Universidade de São Paulo – USP
Renata S. Scalco, Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London
Vinicius Scaramuzzi, Universidade de São Paulo – USP
Vitor Marques Caldas, Universidade de São Paulo – USP
Umbertina Conti Reed, Universidade de São Paulo – USP
Andre Macedo Serafim da Silva, Universidade de São Paulo – USP
Benjamin O'Callaghan, Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London
Rahul Phadke, Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London
Enrico Bugiardini, Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London
Richa Sud, Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London
Samuel McCall, Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London
Michael G. Hanna, Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London
Hanne Poulsen
Roope Männikkö, Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London
Emma Matthews, Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London

No data available

ID: 138771002