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    Monogenic developmental and epileptic encephalopathies of infancy and childhood, a population cohort from Norway by Ida Stenshorne, Ida Stenshorne, Marte Syvertsen, Anette Ramm-Pettersen, Anette Ramm-Pettersen, Susanne Henning, Elisabeth Weatherup, Alf Bjørnstad, Natalia Brüggemann, Torstein Spetalen, Kaja K. Selmer, Kaja K. Selmer, Jeanette Koht

    Published 2022-08-01
    “…The aim of the present study was to describe the clinical picture and to identify genetic causes in a patient cohort with DEE without known etiology, from a Norwegian regional hospital.MethodsSystematic searches of medical records were performed at Drammen Hospital, Vestre Viken Health Trust, to identify patients with epilepsy in the period 1999–2018. …”
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