Exome sequencing followed by large-scale genotyping fails to identify single rare variants of large effect in idiopathic generalized epilepsy

HIGHLIGHTS

• who: ErinnbspL. Heinzen and colleagues from the Subjects and Methods Study Population IGE-affected subjects evaluated in this study were largely recruited through the Epilepsy Genetics (EPIGEN) ConsortiumAcross EPIGEN, subjects are recruited and enrolled by physicians during routine clinical visits across five clinical sites: Erasme Hospital and Universitair Ziekenhuis Gasthuisberg (Belgium), Duke University Medical Center (United States), Beaumont Hospital (Ireland), and the National Hospital for Neurology and Neurosurgery (England). Detailed phenotypic information is collected at the time of enrollment and put into a database in a deidentified manner for the facilitation of genetic association studies. Clinical information . . .
  

   

  

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