Biallelic inherited SCN8A variants, a rare cause of SCN8A-related developmental and epileptic encephalopathy

Eric R. Wengert, Cathrine E. Tronhjem, Jacy L. Wagnon, Katrine M. Johannesen, Hayley Petit, Ilona Krey, Anusha U. Saga, Payal S. Panchal, Samantha M. Strohm, Jörn Lange, Susanne B. Kamphausen, Guido Rubboli, Johannes R. Lemke, Elena Gardella, Manoj K. Patel, Miriam H. Meisler*, Rikke S. Møller

*Corresponding author for this work

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Biochemistry, Genetics and Molecular Biology