Comparison of the frequency of GRIN2A mutations in the different phenotypes of the rolandic spectrum. All three studies find a high frequency in patients with epilepsy-aphasia syndromes including Landau-Kleffner-Syndrome and Continuous Spikes and Waves during slow-wave Sleep (CSWS)
Child Neurology Fellow and epilepsy genetics researcher at the Children’s Hospital of Philadelphia (CHOP), USA and Department of Neuropediatrics, Kiel, Germany
