Article info
PDFReviews
Congenital myasthenic syndromes: an update
- Correspondence to Dr Sarah Finlayson, Department of Clinical Neurology, John Radcliffe Hospital, Oxford, OX3 9DU, UK; sarah.finlayson{at}clneuro.ox.ac.uk
Citation
Congenital myasthenic syndromes: an update
Publication history
- First published March 6, 2013.
Online issue publication
April 14, 2016
Request permissions
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.
Copyright information
Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions
Other content recommended for you
- Clinical features of congenital myasthenic syndrome due to mutations in DPAGT1
- Myasthenia and related disorders of the neuromuscular junction
- Congenital myasthenic syndromes
- Clinical features of the myasthenic syndrome arising from mutations in GMPPB
- Congenital familial myasthenic syndromes: disease and course in an affected dizygotic twin pair
- Update on myasthenia gravis
- Novel ϵ subunit mutation of the muscle acetylcholine receptor causing a slow-channel congenital myasthenic syndrome
- A ‘limb-girdle muscular dystrophy’ responsive to asthma therapy
- An ocular motility conundrum
- An Iranian family with congenital myasthenic syndrome caused by a novel acetylcholine receptor mutation (CHRNE K171X)