Congenital myasthenic syndrome caused by mutations in DPAGT. (2015)
Attributed to:
Disease mechanisms and therapy for inherited disorders of the neuromuscular synapse.
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1016/j.nmd.2014.11.013
PubMed Identifier: 25500013
Publication URI: http://europepmc.org/abstract/MED/25500013
Type: Journal Article/Review
Volume: 25
Parent Publication: Neuromuscular disorders : NMD
Issue: 3
ISSN: 0960-8966