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Article

Clinical Significance of Rare Copy Number Variations in Epilepsy

15 Nov 2011

Abstract excerpt

OBJECTIVE: To perform an extensive search for genomic rearrangements by microarray-based comparative genomic hybridization in patients with epilepsy. DESIGN: Prospective cohort study. SETTING: Epilepsy centers in Italy. PATIENTS: Two hundred seventy-nine patients with unexplained epilepsy, 265 individuals with nonsyndromic mental retardation but no epilepsy, and 246 healthy control subjects were screened by...

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PMID: 22083797
DOI: 10.1001/archneurol.2011.1999

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