VCP mutations are not a major cause of familial amyotrophic lateral sclerosis in the UK. (2015)
Attributed to:
Exome sequencing in motor neuron disease: bioinformatic analyses and biological validation of novel variants
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1016/j.jns.2015.01.021
PubMed Identifier: 25618255
Publication URI: http://europepmc.org/abstract/MED/25618255
Type: Journal Article/Review
Volume: 349
Parent Publication: Journal of the neurological sciences
Issue: 1-2
ISSN: 0022-510X