Further corroboration of distinct functional features in SCN2A variants causing intellectual disability or epileptic phenotypes
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Erschienen in
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In: Molecular Medicine 25 (2019).
- Ereignis
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Veröffentlichung
- (wo)
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Erlangen
- (wer)
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Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU)
- (wann)
-
2019
- Urheber
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Begemann, Anaïs
Acuña, Mario A.
Zweier, Markus
Vincent, Marie
Steindl, Katharina
Bachmann-Gagescu, Ruxandra
Hackenberg, Annette Marie
Abela, Lucia
Plecko, Barbara
Kroell-Seger, Judith
Baumer, Alessandra
Yamakawa, Kazuhiro
Inoue, Yushi
Asadollahi, Reza
Sticht, Heinrich
Zeilhofer, Hanns Ulrich
Rauch, Anita
- URN
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urn:nbn:de:bvb:29-opus4-107100
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:56 MESZ
Datenpartner
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Beteiligte
- Begemann, Anaïs
- Acuña, Mario A.
- Zweier, Markus
- Vincent, Marie
- Steindl, Katharina
- Bachmann-Gagescu, Ruxandra
- Hackenberg, Annette Marie
- Abela, Lucia
- Plecko, Barbara
- Kroell-Seger, Judith
- Baumer, Alessandra
- Yamakawa, Kazuhiro
- Inoue, Yushi
- Asadollahi, Reza
- Sticht, Heinrich
- Zeilhofer, Hanns Ulrich
- Rauch, Anita
- Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU)
Entstanden
- 2019
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