A comprehensive analysis of rare genetic variation in amyotrophic lateral sclerosis in the UK. (2017)
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/10.1093/brain/awx082
PubMed Identifier: 28430856
Publication URI: http://europepmc.org/abstract/MED/28430856
Type: Journal Article/Review
Volume: 140
Parent Publication: Brain : a journal of neurology
Issue: 6
ISSN: 0006-8950