Biallelic inherited SCN8A variants,a rare cause of SCN8A‐related developmental and epileptic encephalopathy |
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| Authors: | 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,J rn Lange,Susanne B. Kamphausen,Guido Rubboli,Johannes R. Lemke,Elena Gardella,Manoj K. Patel,Miriam H. Meisler,Rikke S. M ller |
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| Affiliation: | 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 |
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