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A novel ATP1A2 mutation in a patient with hypokalaemic periodic paralysis and CNS symptoms. (2018)

First Author: Sampedro CastaƱeda M
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