Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. (2011)
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/10.1016/s0140-6736(10)62345-8
PubMed Identifier: 21292315
Publication URI: http://europepmc.org/abstract/MED/21292315
Type: Journal Article/Review
Volume: 377
Parent Publication: Lancet (London, England)
Issue: 9766
ISSN: 0140-6736