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A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations
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Genome wide high density SNP-based linkage analysis of childhood absence epilepsy identifies a susceptibility locus

Barry A Chioza1, Jean Aicardi, Harald Aschauer

  • 1Institute of Child Health, University College London, London, UK. b.chioza@ucl.ac.uk

Epilepsy Research
|October 20, 2009
PubMed

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