Predominantly myalgic phenotype caused by the c.3466G>A p.A1156T mutation in SCN4A gene (2017)
Attributed to:
MICA: MRC Centre for Neuromuscular Diseases
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1212/wnl.0000000000003846
PubMed Identifier: 28330959
Publication URI: http://europepmc.org/abstract/MED/28330959
Type: Journal Article/Review
Parent Publication: Neurology
Issue: 16
ISSN: 0028-3878