GRIN2A

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)

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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