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Article

Diagnostic implications of genetic copy number variation in epilepsy plus

13 Mar 2019

Abstract excerpt

Summary Objective Copy number variations ( CNV s) represent a significant genetic risk for several neurodevelopmental disorders including epilepsy. As knowledge increases, reanalysis of existing data is essential. Reliable estimates of the contribution of CNV s to epilepsies from sizeable populations are not available. Methods We assembled a cohort of 1255 patients with preexisting array comparative genomic...

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PMID: 30866059
DOI: 10.1111/epi.14683

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