A brief report: de novo copy number variants in children with attention deficit hyperactivity disorder

Recent case–control genetic studies of attention deficit hyperactivity disorder (ADHD) have implicated common and rare genetic risk alleles, highlighting the polygenic and complex aetiology of this neurodevelopmental disorder. Studies of other neurodevelopmental disorders, such as autism spectrum di...

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Bibliografiska uppgifter
I publikationen:Transl Psychiatry
Huvudupphovsmän: Martin, Joanna, Hosking, Grace, Wadon, Megan, Agha, Sharifah Shameem, Langley, Kate, Rees, Elliott, Owen, Michael J., O’Donovan, Michael, Kirov, George, Thapar, Anita
Materialtyp: Artigo
Språk:Inglês
Publicerad: Nature Publishing Group UK 2020
Ämnen:
Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC7217839/
https://ncbi.nlm.nih.gov/pubmed/32398668
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41398-020-0821-y
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