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

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  • awy283

    Final published version, 1.29 MB, PDF document

DOI

  • Marisol Sampedro Castañeda, Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London
    • ,
  • Edmar Zanoteli, Universidade de Sao Paulo
    • ,
  • Renata S. Scalco, Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London
    • ,
  • Vinicius Scaramuzzi, Universidade de Sao Paulo
    • ,
  • Vitor Marques Caldas, Universidade de Sao Paulo
    • ,
  • Umbertina Conti Reed, Universidade de Sao Paulo
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  • Andre Macedo Serafim da Silva, Universidade de Sao Paulo
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  • 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
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  • 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
Original languageEnglish
JournalBrain : a journal of neurology
Volume141
Issue12
Pages (from-to)3308-3318
Number of pages11
ISSN0006-8950
DOIs
Publication statusPublished - 1 Dec 2018

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