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Evaluation of familial phenotype deviation to measure the impact of de novo mutations in autism.

Genome Med · 2025 · PMC12366145 · PMID 40836247

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showed a trendno p-value reported
Although most ASD core symptom measures, especially social communication deficits, showed a trend toward attenuated severity in probands carrying dnDIS compared to non-carriers, consistent with previous findings [ 53 ], SRS T-scores were significantly higher in dnDIS carriers (Table 2 ).

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