Clinical Significance of Rare Copy Number Variations in Epilepsy: A Case-Control Survey Using Microarray-Based Comparative Genomic Hybridization - Striano, Pasquale; Coppola, Antonietta; Paravidino, Roberta; Malacarne, Michela; Gimelli, Stefania; Robbiano, Angela; Traverso, Monica; Pezzella, Marianna; Belcastro, Vincenzo; Bianchi, Amedeo; Elia, Maurizio; Falace, Antonio; et al. (Archives of neurology (Chicago), 2012)
Keywords: Adolescent; Adult; Age of Onset; Aged; Biological and medical sciences; Child; Child, Preschool; Cohort Studies; Computational Biology; Diagnostic and Statistical Manual of Mental Disorders; Epilepsy; Epilepsy - genetics; Female; Gene Deletion; Gene Dosage; Gene Duplication; Gene Rearrangement; Genes; Genome-Wide Association Study; Genomics; Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy; Humans; In Situ Hybridization, Fluorescence; Intellectual disabilities; Intellectual Disability - epidemiology; Intellectual Disability - genetics; Italy - epidemiology; Magnetic Resonance Imaging; Male; Medical sciences; Medical screening; Microarray Analysis; Middle Aged; Nervous system (semeiology, syndromes); Nervous System Diseases - epidemiology; Nervous System Diseases - genetics; Neurology; Nucleic Acid Hybridization; Polymerase Chain Reaction; Prospective Studies; Young Adult; Italy; Survey; Nervous system diseases; Comparative genomic hybridization; Copy number; Epilepsy; Central nervous system disease; Cerebral disorder