Mutations in BICD2 cause dominant congenital spinal muscular atrophy and hereditary spastic paraplegia. (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/10.1016/j.ajhg.2013.04.018
PubMed Identifier: 23664120
Publication URI: http://europepmc.org/abstract/MED/23664120
Type: Journal Article/Review
Volume: 92
Parent Publication: American journal of human genetics
Issue: 6
ISSN: 0002-9297