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Whole-Exome Sequencing Reveals Increased Burden of Rare Functional and Disruptive Variants in Candidate Risk Genes in Individuals With Persistent Attention-Deficit/Hyperactivity Disorder
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Author/s
author: Ditte Demontis, Søren Dinesen Østergaard, Ole Mors, Barbara Franke, Anders D. Børglum, Klaus-Peter Lesch
Work details
Publication date
June 2016
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Language
English
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