A novel ATP1A2 mutation in a patient with hypokalaemic periodic paralysis and CNS symptoms. (2018)
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/awy283
PubMed Identifier: 30423015
Publication URI: http://europepmc.org/abstract/MED/30423015
Type: Journal Article/Review
Volume: 141
Parent Publication: Brain : a journal of neurology
Issue: 12
ISSN: 0006-8950