Global characterization of copy number variants in epilepsy patients from whole genome sequencing.

PLoS Genet · 2018 · PMC5978987 · PMID 29649218

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nominally significantno p-value reported

The GABRD gene had the strongest and only nominally significant association with four non-coding deletions among the 198 epileptic patients and none in the 301 controls.

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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.