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- Q56986291 description "article scientifique publié en 2016" @default.
- Q56986291 description "article" @default.
- Q56986291 description "im Juni 2016 veröffentlichter wissenschaftlicher Artikel" @default.
- Q56986291 description "wetenschappelijk artikel" @default.
- Q56986291 description "наукова стаття, опублікована в червні 2016" @default.
- Q56986291 description "հոդված" @default.
- Q56986291 name "Whole-Exome Sequencing Reveals Increased Burden of Rare Functional and Disruptive Variants in Candidate Risk Genes in Individuals With Persistent Attention-Deficit/Hyperactivity Disorder" @default.
- Q56986291 name "Whole-Exome Sequencing Reveals Increased Burden of Rare Functional and Disruptive Variants in Candidate Risk Genes in Individuals With Persistent Attention-Deficit/Hyperactivity Disorder" @default.
- Q56986291 type Item @default.
- Q56986291 label "Whole-Exome Sequencing Reveals Increased Burden of Rare Functional and Disruptive Variants in Candidate Risk Genes in Individuals With Persistent Attention-Deficit/Hyperactivity Disorder" @default.
- Q56986291 label "Whole-Exome Sequencing Reveals Increased Burden of Rare Functional and Disruptive Variants in Candidate Risk Genes in Individuals With Persistent Attention-Deficit/Hyperactivity Disorder" @default.
- Q56986291 altLabel "Whole-Exome Sequencing Reveals Increased Burden of Rare Functional and Disruptive Variants in Candidate Risk Genes in Individuals With Persistent Attention-Deficit/Hyperactivity Disorder" @default.
- Q56986291 altLabel "Whole-Exome Sequencing Reveals Increased Burden of Rare Functional and Disruptive Variants in Candidate Risk Genes in Individuals With Persistent Attention-Deficit/Hyperactivity Disorder." @default.
- Q56986291 prefLabel "Whole-Exome Sequencing Reveals Increased Burden of Rare Functional and Disruptive Variants in Candidate Risk Genes in Individuals With Persistent Attention-Deficit/Hyperactivity Disorder" @default.
- Q56986291 prefLabel "Whole-Exome Sequencing Reveals Increased Burden of Rare Functional and Disruptive Variants in Candidate Risk Genes in Individuals With Persistent Attention-Deficit/Hyperactivity Disorder" @default.
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- Q56986291 P356 J.JAAC.2016.03.009 @default.
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- Q56986291 P1476 "Whole-Exome Sequencing Reveals Increased Burden of Rare Functional and Disruptive Variants in Candidate Risk Genes in Individuals With Persistent Attention-Deficit/Hyperactivity Disorder" @default.
- Q56986291 P2093 "Andreas Reif" @default.
- Q56986291 P2093 "Francesco Lescai" @default.
- Q56986291 P2093 "Hui Jiang" @default.
- Q56986291 P2093 "Jan K. Buitelaar" @default.
- Q56986291 P2093 "Jieqin Liang" @default.
- Q56986291 P2093 "Jun Wang" @default.
- Q56986291 P2093 "Qibin Li" @default.
- Q56986291 P2093 "Simon Glerup" @default.
- Q56986291 P2093 "Yingrui Li" @default.
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- Q56986291 P356 "10.1016/J.JAAC.2016.03.009" @default.
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- Q56986291 P577 "2016-06-01T00:00:00Z" @default.
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