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Tronhjem, Cathrine E ;
Wagnon, Jacy L...
Wengert , E R , Tronhjem , C E , Wagnon , J L , Johannesen , K M , Petit , H , Krey , I , Saga , A U , Panchal , P S , Strohm , S M , Lange , J , Kamphausen , S B , Rubboli , G , Lemke , J R , Gardella , E , Patel , M K , Meisler , M H & Møller , R S 2019 , ' Biallelic inherited SCN8A variants, a rare cause of SCN8A-related developmental and epileptic encephalopathy ' , Epilepsia , vol. 60 , no. 11 , pp. 2277-2285 . https://doi.org/10.1111/epi.16371.
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2019