Independent estimation of the frequency of rare CNVs in the UK population confirms their role in schizophrenia

BACKGROUND: Several large, rare chromosomal copy number variants (CNVs) have recently been shown to increase risk for schizophrenia and other neuropsychiatric disorders including autism, ADHD, learning difficulties and epilepsy. AIMS: We wanted to examine the frequencies of these schizophrenia-assoc...

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Detalles Bibliográficos
Autores principales: Grozeva, Detelina, Conrad, Donald F., Barnes, Chris P., Hurles, Matthew, Owen, Michael J., O'Donovan, Michael C., Craddock, Nick, Kirov, George
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2012
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3315675/
https://www.ncbi.nlm.nih.gov/pubmed/22130109
http://dx.doi.org/10.1016/j.schres.2011.11.004

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3315675/
https://www.ncbi.nlm.nih.gov/pubmed/22130109
http://dx.doi.org/10.1016/j.schres.2011.11.004

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