Electrophysiologic features of SYT2 mutations causing a treatable neuromuscular syndrome. (2015)
Attributed to:
MICA: MRC Centre for Neuromuscular Diseases
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1212/wnl.0000000000002185
PubMed Identifier: 26519543
Publication URI: http://europepmc.org/abstract/MED/26519543
Type: Journal Article/Review
Volume: 85
Parent Publication: Neurology
Issue: 22
ISSN: 0028-3878