Loss-of-function mutations in SCN4A cause severe foetal hypokinesia or 'classical' congenital myopathy. (2016)
Attributed to:
MICA: MRC Centre for Neuromuscular Diseases
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1093/brain/awv352
PubMed Identifier: 26700687
Publication URI: http://europepmc.org/abstract/MED/26700687
Type: Journal Article/Review
Volume: 139
Parent Publication: Brain : a journal of neurology
Issue: Pt 3
ISSN: 0006-8950