De novo SCN8A and inherited rare CACNA1H variants associated with severe developmental and epileptic encephalopathy
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1756-6606
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Anmerkungen
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online resource.
- Erschienen in
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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
- Urheber
-
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
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
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10.1186/s13041-021-00838-y
- URN
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urn:nbn:de:101:1-2021112220021945223217
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:33 MESZ
Datenpartner
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Beteiligte
- 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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