A recessive Nav1.4 mutation underlies congenital myasthenic syndrome with periodic paralysis. (2016)

First Author: Habbout K

Attributed to: Periodic paralysis: from molecules to mice funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1212/wnl.0000000000002264

PubMed Identifier: 26659129

Publication URI: http://europepmc.org/abstract/MED/26659129

Type: Journal Article/Review

Volume: 86

Parent Publication: Neurology

Issue: 2

ISSN: 0028-3878