Barely Significant
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De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability.

Mol Psychiatry · 2014 · PMC4031262 · PMID 24776741

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may be significantno p-value reported
We also found that genes with potentially functional mutations ranked significantly less intolerant to rare variation, complementing recently proposed hypotheses that DNMs may be significant risk factors for sporadic schizophrenia 16 , 47 .

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