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

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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
Nummer12
Sider (fra-til)3308-3318
Antal sider11
ISSN0006-8950
DOI
StatusUdgivet - 1 dec. 2018

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