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Predominantly myalgic phenotype caused by the c.3466G>A p.A1156T mutation in SCN4A gene. (2017)

First Author: Palmio J

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.0000000000003846

PubMed Identifier: 28330959

Publication URI: http://europepmc.org/abstract/MED/28330959

Type: Journal Article/Review

Volume: 88

Parent Publication: Neurology

Issue: 16

ISSN: 0028-3878