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Congenital myopathy with "corona" fibres, selective muscle atrophy, and craniosynostosis associated with novel recessive mutations in SCN4A. (2017)

First Author: Gonorazky HD

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

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.nmd.2017.02.001

PubMed Identifier: 28262468

Publication URI: http://europepmc.org/abstract/MED/28262468

Type: Journal Article/Review

Volume: 27

Parent Publication: Neuromuscular disorders : NMD

Issue: 6

ISSN: 0960-8966