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

First Author: Palmio J
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

Volume: 88

Parent Publication: Neurology

Issue: 16

ISSN: 0028-3878