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Congenital myasthenic syndrome caused by mutations in DPAGT. (2015)

First Author: Klein A

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