Biallelic inherited SCN8A variants, a rare cause of SCN8A‐related developmental and epileptic encephalopathy von Wengert, Eric R., Tronhjem, Cathrine E., Wagnon, Jacy L., Johannesen, Katrine M., Petit, Hayley, Krey, Ilona, Saga, Anusha U., Panchal, Payal S., Strohm, Samantha M., Lange, Jörn, Kamphausen, Susanne B., Rubboli, Guido, Lemke, Johannes R., Gardella, Elena, Patel, Manoj K., Meisler, Miriam H., Møller, Rikke S.

Volltext