Congenital myopathy with "corona" fibres, selective muscle atrophy, and craniosynostosis associated with novel recessive mutations in SCN4A. (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/10.1016/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