Nebulin (NEB) mutations in a childhood onset distal myopathy with rods and cores uncovered by next generation sequencing. (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/10.1038/ejhg.2013.31
PubMed Identifier: 23443021
Publication URI: http://europepmc.org/abstract/MED/23443021
Type: Journal Article/Review
Volume: 21
Parent Publication: European journal of human genetics : EJHG
Issue: 11
ISSN: 1018-4813