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Integrated Model of De Novo and Inherited Genetic Variants Yields Greater Power to Identify Risk Genes

Published Web Location

http://europepmc.org/articles/PMC3744441?pdf=render
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Abstract

De novo mutations affect risk for many diseases and disorders, especially those with early-onset. An example is autism spectrum disorders (ASD). Four recent whole-exome sequencing (WES) studies of ASD families revealed a handful of novel risk genes, based

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