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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
Research output: Contribution to journal › Journal article › Research › peer-review
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