Genome-wide transcriptome profiling reveals the functional impact of rare de novo and recurrent CNVs in autism spectrum disorders.

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Published in Am J Hum Genet on June 21, 2012

Authors

Rui Luo1, Stephan J Sanders, Yuan Tian, Irina Voineagu, Ni Huang, Su H Chu, Lambertus Klei, Chaochao Cai, Jing Ou, Jennifer K Lowe, Matthew E Hurles, Bernie Devlin, Matthew W State, Daniel H Geschwind

Author Affiliations

1: Department of Human Genetics, David Geffen School of Medicine, University of California, Los Angeles, 90095, USA.

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