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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| Description | article |
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author: Ditte Demontis Ole Mors Klaus-Peter Lesch Anders D. Børglum Barbara Franke Søren Dinesen Østergaard |
| Publication date | June 2016 |
| Language | English |
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