Barely Significant
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Targeted massively parallel sequencing of autism spectrum disorder-associated genes in a case control cohort reveals rare loss-of-function risk variants.

Mol Autism · 2015 · PMC4504419 · PMID 26185613

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nominally significantno p-value reported
However, investigation of the nominally significant genes can be informative for potential roles of several genes in ASD risk.

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