Novel mutations widen the phenotypic spectrum of slow skeletal/ß-cardiac myosin (MYH7) distal myopathy. (2014)
Attributed to:
MICA: MRC Centre for Neuromuscular Diseases
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1002/humu.22553
PubMed Identifier: 24664454
Publication URI: http://europepmc.org/abstract/MED/24664454
Type: Journal Article/Review
Volume: 35
Parent Publication: Human mutation
Issue: 7
ISSN: 1059-7794