ISPD gene mutations are a common cause of congenital and limb-girdle muscular dystrophies. (2013)
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/aws312
PubMed Identifier: 23288328
Publication URI: http://europepmc.org/abstract/MED/23288328
Type: Journal Article/Review
Volume: 136
Parent Publication: Brain : a journal of neurology
Issue: Pt 1
ISSN: 0006-8950