Novel mutations in the C-terminal region of GMPPB causing limb-girdle muscular dystrophy overlapping with congenital myasthenic syndrome. (2017)
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.2017.03.004
PubMed Identifier: 28433477
Publication URI: http://europepmc.org/abstract/MED/28433477
Type: Journal Article/Review
Volume: 27
Parent Publication: Neuromuscular disorders : NMD
Issue: 6
ISSN: 0960-8966