NRXN1 deletions and IGE. 5/1500 IGE patients with NRXN1 deletions were identified in the study by Møller and collaborators. 3/5 probands carried additional, possibly pathogenic structural genomic variants
Child Neurology Fellow and epilepsy genetics researcher at the Children’s Hospital of Philadelphia (CHOP), USA and Department of Neuropediatrics, Kiel, Germany
