Congenital myasthenic syndrome due to choline acetyltransferase mutations in infants: clinical suspicion and comprehensive electrophysiological assessment are important for early diagnosis. (2014)
Attributed to:
MICA: MRC Centre for Neuromuscular Diseases
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1177/0883073812470000
PubMed Identifier: 23292760
Publication URI: http://europepmc.org/abstract/MED/23292760
Type: Journal Article/Review
Volume: 29
Parent Publication: Journal of child neurology
Issue: 3
ISSN: 0883-0738