Barely Significant
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Absence seizures in C3H/HeJ and knockout mice caused by mutation of the AMPA receptor subunit Gria4.

Hum Mol Genet · 2008 · PMC2405903 · PMID 18316356

1
hedged sentence
closest p
boldest claim

The sentences

highly significantno p-value reported
By utilizing genetic markers to distinguish substrains, we determined that there was a highly significant association with SWD incidence, indicating that the locus of major effect maps to centromeric Chromosome 9 (Fig. 1 ), consistent with it being spkw1 .

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