Genome-wide analysis shows increased frequency of CNV deletions in Dutch schizophrenia patients

BACKGROUND: Since 2008 multiple studies have reported on copy number variations (CNVs) in schizophrenia. However, many regions are unique events with minimal overlap between studies. This makes it difficult to gain a comprehensive overview of all CNVs involved in the aetiology of schizophrenia. We p...

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Hlavní autoři: Buizer-Voskamp, Jacobine E, Muntjewerff, Jan-Willem, Strengman, Eric, Sabatti, Chiara, Stefansson, Hreinn, Vorstman, Jacob AS, Ophoff, Roel A
Médium: Artigo
Jazyk:Inglês
Vydáno: 2011
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On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3137747/
https://ncbi.nlm.nih.gov/pubmed/21489405
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.biopsych.2011.02.015
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