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A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease risk. (2013)

First Author: Chapman J

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1093/hmg/dds476

PubMed Identifier: 23148125

Publication URI: http://europepmc.org/abstract/MED/23148125

Type: Journal Article/Review

Volume: 22

Parent Publication: Human molecular genetics

Issue: 4

ISSN: 0964-6906