Clinical features of congenital myasthenic syndrome due to mutations inDPAGT1-Reference-Cited by-同舟云学术

Clinical features of congenital myasthenic syndrome due to mutations inDPAGT1

Published:2013-02-27 Issue:10 Volume:84 Page:1119-1125
ISSN:0022-3050
Container-title:Journal of Neurology, Neurosurgery & Psychiatry
language:en
Short-container-title:J Neurol Neurosurg Psychiatry

Author:

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

Publisher

BMJ

Subject

Psychiatry and Mental health,Clinical Neurology,Surgery

Reference28 articles.

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3. 186th ENMC international workshop: congenital myasthenic syndromes 24–26 June 2011, Naarden, The Netherlands;Chaouch;Neuromuscul Disord,2012

4. The congenital myasthenic syndromes;Palace;J Neuroimmunol,2008

5. Mutations in DPAGT1 cause a limb-girdle congenital myasthenic syndrome with tubular aggregates;Belaya;Am J Hum Genet,2012

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