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Congenital myasthenic syndrome due to DPAGT1 mutations mimicking congenital myopathy in an Irish family.
Bogdanova-Mihaylova, P; Murphy, R P J; Alexander, M D; McHugh, J C; Foley, A Reghan; Brett, F; Murphy, S M.
Afiliación
  • Bogdanova-Mihaylova P; Department of Neurology, Adelaide and Meath Hospitals incorporating the National Children's Hospital, Dublin.
  • Murphy RPJ; Department of Neurology, Adelaide and Meath Hospitals incorporating the National Children's Hospital, Dublin.
  • Alexander MD; Department of Clinical Neurophysiology, Adelaide and Meath Hospitals incorporating the National Children's Hospital, Dublin.
  • McHugh JC; Academic Unit of Neurology, Trinity College Dublin, Dublin, Ireland.
  • Foley AR; Department of Clinical Neurophysiology, Adelaide and Meath Hospitals incorporating the National Children's Hospital, Dublin.
  • Brett F; Academic Unit of Neurology, Trinity College Dublin, Dublin, Ireland.
  • Murphy SM; Neuromuscular and Neurogenetic Disorders of Childhood Section, Neurogenetics Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.
Eur J Neurol ; 25(2): e22-e23, 2018 02.
Article en En | MEDLINE | ID: mdl-29356258
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Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Eur J Neurol Asunto de la revista: NEUROLOGIA Año: 2018 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Eur J Neurol Asunto de la revista: NEUROLOGIA Año: 2018 Tipo del documento: Article