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De novo SCN8A and inherited rare CACNA1H variants associated with severe developmental and epileptic encephalopathy.

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Bibliographic Details
Title: De novo SCN8A and inherited rare CACNA1H variants associated with severe developmental and epileptic encephalopathy.
Authors: Stringer, Robin N.1,2 (AUTHOR), Jurkovicova-Tarabova, Bohumila3 (AUTHOR), Souza, Ivana A.4 (AUTHOR), Ibrahim, Judy5 (AUTHOR), Vacik, Tomas6 (AUTHOR), Fathalla, Waseem Mahmoud7 (AUTHOR), Hertecant, Jozef5,8 (AUTHOR), Zamponi, Gerald W.4 (AUTHOR), Lacinova, Lubica3 (AUTHOR), Weiss, Norbert1,2,3,6 (AUTHOR) nalweiss@gmail.com
Source: Molecular Brain. 8/16/2021, Vol. 14 Issue 1, p1-5. 5p.
Database: Academic Search Ultimate
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Description
ISSN:17566606
DOI:10.1186/s13041-021-00838-y