De novo mutations revealed by whole-exome sequencing are strongly associated with autism




De novo mutations revealed by whole-exome sequencing are strongly associated with autism by Stephan J. Sanders et. al.. published in Nature 485, 237–241 (10 May 2012) doi:10.1038/nature10945. Abstract Multiple studies have confirmed the contribution of rare de novo copy number variations to the risk for autism spectrum disorders. But whereas de novo single nucleotide variants […]