Novel mutations in human and mouse SCN4A implicate AMPK in myotonia and periodic paralysis. (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/10.1093/brain/awu292
PubMed Identifier: 25348630
Publication URI: http://europepmc.org/abstract/MED/25348630
Type: Journal Article/Review
Volume: 137
Parent Publication: Brain : a journal of neurology
Issue: Pt 12
ISSN: 0006-8950