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De novo SCN8A and inherited rare CACNA1H variants associated with severe developmental and epileptic encephalopathy by Robin N. Stringer, Bohumila Jurkovicova-Tarabova, Ivana A. Souza, Judy Ibrahim, Tomas Vacik, Waseem Mahmoud Fathalla, Jozef Hertecant, Gerald W. Zamponi, Lubica Lacinova, Norbert Weiss
Published 2021-08-01
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