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Congenital myasthenic syndrome due to a TOR1AIP1 mutation: a new disease pathway for impaired synaptic transmission.
Cossins, Judith; Webster, Richard; Maxwell, Susan; Rodríguez Cruz, Pedro M; Knight, Ravi; Llewelyn, John Gareth; Shin, Ji-Yeon; Palace, Jacqueline; Beeson, David.
Afiliación
  • Cossins J; Neurosciences Group, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, University of Oxford, Oxford OX3 9DS, UK.
  • Webster R; Neurosciences Group, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, University of Oxford, Oxford OX3 9DS, UK.
  • Maxwell S; Neurosciences Group, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, University of Oxford, Oxford OX3 9DS, UK.
  • Rodríguez Cruz PM; Neurosciences Group, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, University of Oxford, Oxford OX3 9DS, UK.
  • Knight R; Department of Clinical Neurology, John Radcliffe Hospital, Oxford OX3 9DU, UK.
  • Llewelyn JG; Neurology Department, University Hospital of Wales, Heath Park, Cardiff CF14 4XW, UK.
  • Shin JY; Department of Medicine, Columbia University Medical Centre, New York, NY 10032, USA.
  • Palace J; Department of Clinical Neurology, John Radcliffe Hospital, Oxford OX3 9DU, UK.
  • Beeson D; Neurosciences Group, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, University of Oxford, Oxford OX3 9DS, UK.
Brain Commun ; 2(2): fcaa174, 2020.
Article en En | MEDLINE | ID: mdl-33215087
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Texto completo: 1 Colección: 01-internacional Tipo de estudio: Prognostic_studies Idioma: En Revista: Brain Commun Año: 2020 Tipo del documento: Article País de afiliación: Reino Unido
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Tipo de estudio: Prognostic_studies Idioma: En Revista: Brain Commun Año: 2020 Tipo del documento: Article País de afiliación: Reino Unido