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Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis
BACKGROUND: Large, rare chromosomal deletions and duplications known as copy number variants (CNVs) have been implicated in neurodevelopmental disorders similar to attention-deficit hyperactivity disorder (ADHD). We aimed to establish whether burden of CNVs was increased in ADHD, and to investigate...
Autores principales: | Williams, Nigel M, Zaharieva, Irina, Martin, Andrew, Langley, Kate, Mantripragada, Kiran, Fossdal, Ragnheidur, Stefansson, Hreinn, Stefansson, Kari, Magnusson, Pall, Gudmundsson, Olafur O, Gustafsson, Omar, Holmans, Peter, Owen, Michael J, O'Donovan, Michael, Thapar, Anita |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Lancet Publishing Group
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2965350/ https://www.ncbi.nlm.nih.gov/pubmed/20888040 http://dx.doi.org/10.1016/S0140-6736(10)61109-9 |
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