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Using large clinical data sets to infer pathogenicity for rare copy number variants in autism cohorts
Published Web Location
http://europepmc.org/articles/PMC3720840?pdf=renderNo data is associated with this publication.
Abstract
Copy number variants (CNVs) have a major role in the etiology of autism spectrum disorders (ASD), and several of these have reached statistical significance in case-control analyses. Nevertheless, current ASD cohorts are not large enough to detect very rar
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