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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Publication year
2016
Author(s)
Demontis, D.
Lescai, F.
Borglum, A.
Glerup, S.
Ostergaard, S.D.
Mors, O.
Li, Q.
Liang, J.Q.
Jiang, H.
Li, Y.
Wang, J
Lesch, K.P.
Reif, A.
Buitelaar, J.K.
Franke, B.
Source
Journal of the American Academy of Child and Adolescent Psychiatry, 55, 6, (2016), pp. 521-3
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Publication type
Article / Letter to editor
If a DOI or any other persistent identifier is unavailable, please use the following repository identifier to link to this item: https://hdl.handle.net/2066/168279   https://hdl.handle.net/2066/168279
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