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

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  • awy283

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DOI

    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
OriginalsprogEngelsk
TidsskriftBrain : a journal of neurology
Vol/bind141
Tidsskriftsnummer12
Sider (fra-til)3308-3318
Antal sider11
ISSN0006-8950
DOI
StatusUdgivet - 1 dec. 2018

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