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

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1756-6606

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: De novo SCN8A and inherited rare CACNA1H variants associated with severe developmental and epileptic encephalopathy ; volume:14 ; number:1 ; day:16 ; month:8 ; year:2021 ; pages:1-5 ; date:12.2021
Molecular brain ; 14, Heft 1 (16.8.2021), 1-5, 12.2021

Creator: Stringer, Robin N.
Jurkovicova-Tarabova, Bohumila
Souza, Ivana A.
Ibrahim, Judy
Vacik, Tomas
Fathalla, Waseem Mahmoud
Hertecant, Jozef
Zamponi, Gerald Werner
Lacinova, Lubica
Weiss, Norbert

Contributor: SpringerLink (Online service)

DOI: 10.1186/s13041-021-00838-y

URN: urn:nbn:de:101:1-2021112220021945223217

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:33 AM CEST

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Associated

Stringer, Robin N.
Jurkovicova-Tarabova, Bohumila
Souza, Ivana A.
Ibrahim, Judy
Vacik, Tomas
Fathalla, Waseem Mahmoud
Hertecant, Jozef
Zamponi, Gerald Werner
Lacinova, Lubica
Weiss, Norbert
SpringerLink (Online service)

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

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Other Objects (12)

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