Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease. (2012)
Attributed to:
ERANET 1 NEURON 3: 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/10.1093/hmg/dds335
PubMed Identifier: 22892372
Publication URI: http://europepmc.org/abstract/MED/22892372
Type: Journal Article/Review
Volume: 21
Parent Publication: Human molecular genetics
Issue: 22
ISSN: 0964-6906