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Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease (2012)

First Author: Keller M

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

Parent Publication: Human Molecular Genetics

Issue: 22

ISSN: 0964-6906