Copy number variation in a hospital-based cohort of children with epilepsy
Author:
Affiliation:
1. Departments of Neurology; University Medical Center Groningen; University of Groningen; Groningen the Netherlands
2. Department of Genetics; University Medical Center Groningen; University of Groningen; Groningen the Netherlands
Funder
Universidade Católica de Brasília
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Reference33 articles.
1. The hidden genetics of epilepsy-a clinically important new paradigm;Thomas;Nat Rev Neurol,2014
2. Advancing epilepsy genetics in the genomic era;Myers;Genome Med,2015
3. Copy number and SNP arrays in clinical diagnostics;Schaaf;Annu Rev Genomics Hum Genet,2011
4. Deletions or duplications in KCNQ2 can cause benign familial neonatal seizures;Heron;J Med Genet,2007
5. Genetic testing in benign familial epilepsies of the first year of life: clinical and diagnostic significance;Zara;Epilepsia,2013
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