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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Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: Lancet Publishing Group 2010
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Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2965350/
https://ncbi.nlm.nih.gov/pubmed/20888040
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/S0140-6736(10)61109-9
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