Congenital myasthenic syndrome due to DPAGT1 mutations mimicking congenital myopathy in an Irish family. (22nd January 2018)

Record Type:: Journal Article
Title:: Congenital myasthenic syndrome due to DPAGT1 mutations mimicking congenital myopathy in an Irish family. (22nd January 2018)
Main Title:: Congenital myasthenic syndrome due to DPAGT1 mutations mimicking congenital myopathy in an Irish family
Authors:: Bogdanova‐Mihaylova, P.
Murphy, R. P. J.
Alexander, M. D.
McHugh, J. C.
Foley, A. Reghan
Brett, F.
Murphy, S. M.
Abstract:
Is Part Of:: European journal of neurology. Volume 25:Number 2(2018)
Journal:: European journal of neurology
Issue:: Volume 25:Number 2(2018)
Issue Display:: Volume 25, Issue 2 (2018)
Year:: 2018
Volume:: 25
Issue:: 2
Issue Sort Value:: 2018-0025-0002-0000
Page Start:: e22
Page End:: e23
Publication Date:: 2018-01-22
Subjects:: congenital myasthenic syndrome -- DPAGT1
Neurology -- Periodicals
Nervous system -- Diseases -- Periodicals
616.8
Journal URLs:: http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1468-1331 ↗
http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1111/ene.13532 ↗
Languages:: English
ISSNs:: 1351-5101
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 3829.731680
British Library DSC - BLDSS-3PM
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Ingest File:: 23362.xml