A novel ATP1A2 mutation in a patient with hypokalaemic periodic paralysis and CNS symptoms (2018)
- Authors:
- USP affiliated authors: ZANOTELI, EDMAR - FM ; REED, UMBERTINA CONTI - FM
- Unidade: FM
- DOI: 10.1093/brain/awy283
- Subjects: DOENÇAS MUSCULARES; POTÁSSIO; PARESIA; PROTEÍNAS DE TRANSPORTE; MUTAÇÃO GENÉTICA
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Source:
- Status:
- Artigo aberto em periódico híbrido (Hybrid Open Access)
- Versão do Documento:
- Versão publicada (Published version)
- Acessar versão aberta:
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ABNT
CASTANEDA, Marisol Sampedro et al. A novel ATP1A2 mutation in a patient with hypokalaemic periodic paralysis and CNS symptoms. Brain, v. 141, p. 3308-3318, 2018Tradução . . Disponível em: https://doi.org/10.1093/brain/awy283. Acesso em: 14 abr. 2026. -
APA
Castaneda, M. S., Zanoteli, E., Scalco, R. S., Scaramuzzi, V., Caldas, V. M., Reed, U. C., et al. (2018). A novel ATP1A2 mutation in a patient with hypokalaemic periodic paralysis and CNS symptoms. Brain, 141, 3308-3318. doi:10.1093/brain/awy283 -
NLM
Castaneda MS, Zanoteli E, Scalco RS, Scaramuzzi V, Caldas VM, Reed UC, Silva AMS da, O'callaghan B, Phadke R, Bugiardini E. A novel ATP1A2 mutation in a patient with hypokalaemic periodic paralysis and CNS symptoms [Internet]. Brain. 2018 ; 141 3308-3318.[citado 2026 abr. 14 ] Available from: https://doi.org/10.1093/brain/awy283 -
Vancouver
Castaneda MS, Zanoteli E, Scalco RS, Scaramuzzi V, Caldas VM, Reed UC, Silva AMS da, O'callaghan B, Phadke R, Bugiardini E. A novel ATP1A2 mutation in a patient with hypokalaemic periodic paralysis and CNS symptoms [Internet]. Brain. 2018 ; 141 3308-3318.[citado 2026 abr. 14 ] Available from: https://doi.org/10.1093/brain/awy283 - Common and variable clinical, histological, and imaging findings of recessive RYR1-related centronuclear myopathy patients
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