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Ataxia and Action Myoclonus Related to Novel Mutations in ATP13A2 Gene.
Manrique, Leire; Sánchez-Rodríguez, Antonio; Pelayo-Negro, Ana L; Corral-Juan, Marc; Matilla-Dueñas, Antoni; Infante, Jon.
Afiliação
  • Manrique L; Service of Neurology University Hospital "Marqués de Valdecilla (IDIVAL)", University of Cantabria, and "Centro de Investigación Biomédica en Red de Enfermedades, Neurodegenerativas (CIBERNED)" Santander Spain.
  • Sánchez-Rodríguez A; Service of Neurology University Hospital "Marqués de Valdecilla (IDIVAL)", University of Cantabria, and "Centro de Investigación Biomédica en Red de Enfermedades, Neurodegenerativas (CIBERNED)" Santander Spain.
  • Pelayo-Negro AL; Service of Neurology University Hospital "Marqués de Valdecilla (IDIVAL)", University of Cantabria, and "Centro de Investigación Biomédica en Red de Enfermedades, Neurodegenerativas (CIBERNED)" Santander Spain.
  • Corral-Juan M; Neurogenetics Laboratory, Functional and Translational Neurogenetics Unit, Department of Neuroscience, Germans Trias i Pujol Research Institute (IGTP) Universitat Autònoma de Barcelona-Can Ruti Campus Barcelona Spain.
  • Matilla-Dueñas A; Neurogenetics Laboratory, Functional and Translational Neurogenetics Unit, Department of Neuroscience, Germans Trias i Pujol Research Institute (IGTP) Universitat Autònoma de Barcelona-Can Ruti Campus Barcelona Spain.
  • Infante J; Service of Neurology University Hospital "Marqués de Valdecilla (IDIVAL)", University of Cantabria, and "Centro de Investigación Biomédica en Red de Enfermedades, Neurodegenerativas (CIBERNED)" Santander Spain.
Mov Disord Clin Pract ; 8(6): 969-971, 2021 Aug.
Article em En | MEDLINE | ID: mdl-34405108
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article
Texto completo
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PubMed Links
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article