Barely Significant
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Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial model.

Mol Autism · 2018 · PMC6293633 · PMID 30564305

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not yet significantno p-value reported
Although not yet significant, RALGAPB is also a promising risk gene for follow-up as recurrent LGD DNMs were identified in ASD.

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