Myasthenic congenital myopathy from recessive mutations at a single residue in Na V 1.4 (2019)

First Author: Elia N

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.0000000000007185

PubMed Identifier: 30824560

Publication URI: http://europepmc.org/abstract/MED/30824560

Type: Journal Article/Review

Parent Publication: Neurology

Issue: 13

ISSN: 0028-3878