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Article

Analysis of rare copy number variation in absence epilepsies

23 Mar 2016

Abstract excerpt

OBJECTIVE: To identify shared genes and pathways between common absence epilepsy (AE) subtypes (childhood absence epilepsy [CAE], juvenile absence epilepsy [JAE], and unclassified absence epilepsy [UAE]) that may indicate common mechanisms for absence seizure generation and potentially a diagnostic continuum. METHODS: We used high-density single-nucleotide polymorphism arrays to analyze genome-wide rare copy...

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PMID: 27123475
DOI: 10.1212/nxg.0000000000000056

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