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Mutations in GMPPB cause congenital myasthenic syndrome and bridge myasthenic disorders with dystroglycanopathies. (2015)

First Author: Belaya K

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/10.1093/brain/awv185

PubMed Identifier: 26133662

Publication URI: http://europepmc.org/abstract/MED/26133662

Type: Journal Article/Review

Volume: 138

Parent Publication: Brain : a journal of neurology

Issue: Pt 9

ISSN: 0006-8950