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J Am Acad Child Adolesc Psychiatry. 2016 Jun;55(6):521-3. doi: 10.1016/j.jaac.2016.03.009.

Whole-Exome Sequencing Reveals Increased Burden of Rare Functional and Disruptive Variants in Candidate Risk Genes in Individuals With Persistent Attention-Deficit/Hyperactivity Disorder.

Author information

1
Aarhus University, Aarhus, Denmark. Electronic address: ditte@biomed.au.dk.
2
Aarhus University, Aarhus, Denmark.
3
Aarhus University Hospital, Risskov, Denmark.
4
BGI-Shenzhen, Shenzhen, China.
5
University of Würzburg, Würzburg, Germany.
6
Goethe University, Frankfurt, Germany.
7
Radboud University Medical Center, Nijmegen, The Netherlands.
PMID:
27238071
DOI:
10.1016/j.jaac.2016.03.009
[Indexed for MEDLINE]

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