Further corroboration of distinct functional features in SCN2A variants causing intellectual disability or epileptic phenotypes

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1528-3658

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Further corroboration of distinct functional features in SCN2A variants causing intellectual disability or epileptic phenotypes ; volume:25 ; number:1 ; day:27 ; month:2 ; year:2019 ; pages:1-15 ; date:12.2019
Molecular medicine ; 25, Heft 1 (27.2.2019), 1-15, 12.2019

Creator: 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

Contributor: SpringerLink (Online service)

DOI: 10.1186/s10020-019-0073-6

URN: urn:nbn:de:101:1-2019032415394614590161

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

Last update: 14.08.2025, 10:48 AM CEST

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Associated

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
SpringerLink (Online service)

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Further corroboration of distinct functional features in SCN2A variants causing intellectual disability or epileptic phenotypes

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Other Objects (12)

Further corroboration of distinct functional features in SCN2A variants causing intellectual disability or epileptic phenotypes

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