Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study.

Brain · 2010 · PMC2892941 · PMID 20522523

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closest p

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borderline significantno p-value reported

We did detect a slight excess of SNPs with borderline significant P -values, and our most associated SNPs suggest multiple independent signals clustered in the same genomic region.

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Quoted from the open-access full text in Europe PMC under the licence the publisher applied. The sentence is reproduced exactly as published; the emphasis is ours.