Barely Significant
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Rates of contributory de novo mutation in high and low-risk autism families.

Commun Biol · 2021 · PMC8410909 · PMID 34471188

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only marginally significantno p-value reported
The aggregated AD for the affected children in the multiplex AGRE families is only marginally significant and its magnitude is a quarter of the AD for the simplex families in SSC.

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