Barely Significant
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Genomic architecture of aggression: rare copy number variants in intermittent explosive disorder.

Am J Med Genet B Neuropsychiatr Genet · 2011 · PMC3168586 · PMID 21812102

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highly significantno p-value reported
DISCUSSION In this study we aimed to determine whether rare pathogenic CNVs are a predisposing factor for impulsive aggressive behavior, due to growing evidence that genomic architecture is highly significant to human biology and disease [Marques-Bonet et al., 2009 ; Mefford and Eichler, 2009 ].

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