Biallelic inherited SCN8A variants, a rare cause of SCN8A ‐related developmental and epileptic encephalopathy
Journal article published in 2019 by
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
and other authors.
,
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
and other authors.
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