NRXN1.001

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

Ingo Helbig

Child Neurology Fellow and epilepsy genetics researcher at the Children’s Hospital of Philadelphia (CHOP), USA and Department of Neuropediatrics, Kiel, Germany

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