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Using large clinical data sets to infer pathogenicity for rare copy number variants in autism cohorts

  • Author(s): State, Matthew
  • Sanders, Stephan
  • Moreno-De-Luca, D
  • Sanders, SJ
  • Willsey, AJ
  • Mulle, JG
  • Lowe, JK
  • Geschwind, DH
  • State, MW
  • Martin, CL
  • Ledbetter, DH
  • et al.

Published Web Location

http://europepmc.org/articles/PMC3720840?pdf=render
No 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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