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

J Am Acad Child Adolesc Psychiatry. 2016 Jun;55(6):521-3. doi: 10.1016/j.jaac.2016.03.009.
No abstract available

Publication types

  • Letter

MeSH terms

  • Attention Deficit Disorder with Hyperactivity / genetics*
  • Exome*
  • Genetic Predisposition to Disease
  • Genotype
  • Humans
  • Risk