Barely Significant
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The role of common genetic variation in presumed monogenic epilepsies.

EBioMedicine · 2022 · PMC9188960 · PMID 35679801

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Contrastingly, PRS analysis for ‘GGE’ did not reach statistical significance in the DDD, Irish Lighthouse, or Genomics England cohorts, all of which had a broader ‘epilepsy with ID’ phenotype, rather than exclusively DEE ( Figure 1 ).

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