2009•Epilepsy & BehaviorRequires access

SCN1A mutation screening in adult patients with Lennox–Gastaut syndrome features

Kaja Kristine Selmer, Caroline Lund, Kristin Brandal, Dag E. Undlien, Eylert Brodtkorb

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Key concepts: Dravet syndrome, Lennox–Gastaut syndrome, Epilepsy, Myoclonic epilepsy, Mutation, Epilepsy syndromes, Multiplex ligation-dependent probe amplification, Medicine

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SCN1A mutation screening in adult patients with Lennox–Gastaut syndrome features — Research Paper | ScholarLens