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DAWN: A framework to identify autism genes and subnetworks using gene expression and genetics

Published Web Location

http://europepmc.org/articles/PMC4016412?pdf=render
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Abstract

Background: De novo loss-of-function (dnLoF) mutations are found twofold more often in autism spectrum disorder (ASD) probands than their unaffected siblings. Multiple independent dnLoF mutations in the same gene implicate the gene in risk and hence provid

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