Clinical features of congenital myasthenic syndrome due to mutations in DPAGT1

Sarah Finlayson; Jacqueline Palace; Katsiaryna Belaya; Timothy J Walls; Fiona Norwood; Georgina Burke; Janice L Holton; Samuel I Pascual-Pascual; Judith Cossins; David Beeson

doi:10.1136/jnnp-2012-304716

Article info

Neuromuscular

Research paper

Clinical features of congenital myasthenic syndrome due to mutations in DPAGT1

Authors

Sarah Finlayson Neurosciences Group, Nuffield Department of Clinical Neurosciences, Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, UK Nuffield Department of Clinical Neurosciences, John Radcliffe Hospital, Oxford, UK PubMed articles Google scholar articles
Jacqueline Palace Nuffield Department of Clinical Neurosciences, John Radcliffe Hospital, Oxford, UK PubMed articles Google scholar articles
Katsiaryna Belaya Neurosciences Group, Nuffield Department of Clinical Neurosciences, Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, UK PubMed articles Google scholar articles
Timothy J Walls Department of Neurology, Regional Neurosciences Centre, Newcastle General Hospital, Newcastle upon Tyne, UK PubMed articles Google scholar articles
Fiona Norwood Department of Neurology, King's College Hospital NHS Foundation Trust, London, UK PubMed articles Google scholar articles
Georgina Burke Wessex Neurological Centre, Southampton General Hospital, Southampton, UK PubMed articles Google scholar articles
Janice L Holton Department of Molecular Neuroscience, UCL Institute of Neurology, London, UK PubMed articles Google scholar articles
Samuel I Pascual-Pascual Servicio de Neurologia Pediátrica, Hospital Universitario La Paz, Departamento de Pediatria, Universidad Autónoma de Madrid, Madrid, Spain PubMed articles Google scholar articles
Judith Cossins Neurosciences Group, Nuffield Department of Clinical Neurosciences, Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, UK PubMed articles Google scholar articles
David Beeson Neurosciences Group, Nuffield Department of Clinical Neurosciences, Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, UK PubMed articles Google scholar articles

Correspondence to Dr Sarah Finlayson, Nuffield Department of Clinical Neurosciences, John Radcliffe Hospital, Oxford OX3 9DU, UK; sarah.finlayson{at}clneuro.ox.ac.uk

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Citation

Finlayson S, Palace J, Belaya K, et al

Clinical features of congenital myasthenic syndrome due to mutations in DPAGT1

Journal of Neurology, Neurosurgery & Psychiatry 2013;84:1119-1125.

Publication history

Received December 4, 2012
Revised January 25, 2013
Accepted January 28, 2013
First published February 27, 2013.

Online issue publication

April 13, 2016

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