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...

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Detalles Bibliográficos
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
Formato: Texto
Lenguaje:English
Publicado: Lancet Publishing Group 2010
Materias:
Articles
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

Internet

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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