Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis. (2016)
Attributed to:
Identification of copy number variants in familial and pathologically proven PD
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1038/ng.3622
PubMed Identifier: 27455348
Publication URI: http://europepmc.org/abstract/MED/27455348
Type: Journal Article/Review
Volume: 48
Parent Publication: Nature genetics
Issue: 9
ISSN: 1061-4036