Mutations in GFPT1 that underlie limb-girdle congenital myasthenic syndrome result in reduced cell-surface expression of muscle AChR. (2013)
Attributed to:
MICA: MRC Centre for Neuromuscular Diseases
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1093/hmg/ddt145
PubMed Identifier: 23569079
Publication URI: http://europepmc.org/abstract/MED/23569079
Type: Journal Article/Review
Volume: 22
Parent Publication: Human molecular genetics
Issue: 14
ISSN: 0964-6906