Further corroboration of distinct functional features in SCN2A variants causing intellectual disability or epileptic phenotypes:
Gespeichert in:
| Hauptverfasser: | , , , , , , , , , , , , , , , , |
|---|---|
| Format: | Elektronisch E-Book |
| Sprache: | English |
| Veröffentlicht: |
Erlangen
Friedrich-Alexander-Universität Erlangen-Nürnberg
2019
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| Schlagworte: | |
| Online-Zugang: | Volltext Volltext Volltext |
| Beschreibung: | 1 Online-Ressource |
Internformat
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| 700 | 1 | |a Zweier, Markus |e Verfasser |4 aut | |
| 700 | 1 | |a Vincent, Marie |e Verfasser |4 aut | |
| 700 | 1 | |a Steindl, Katharina |e Verfasser |4 aut | |
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| 700 | 1 | |a Zeilhofer, Hanns Ulrich |e Verfasser |4 aut | |
| 700 | 1 | |a Rauch, Anita |e Verfasser |4 aut | |
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Datensatz im Suchindex
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| author | Begemann, Anaïs Acuña, Mario A. Zweier, Markus Vincent, Marie Steindl, Katharina Bachmann-Gagescu, Ruxandra Hackenberg, Annette Abela, Lucia Plecko, Barbara Kroell-Seger, Judith Baumer, Alessandra Yamakawa, Kazuhiro Inoue, Yushi Asadollahi, Reza Sticht, Heinrich Zeilhofer, Hanns Ulrich Rauch, Anita |
| author_facet | Begemann, Anaïs Acuña, Mario A. Zweier, Markus Vincent, Marie Steindl, Katharina Bachmann-Gagescu, Ruxandra Hackenberg, Annette Abela, Lucia Plecko, Barbara Kroell-Seger, Judith Baumer, Alessandra Yamakawa, Kazuhiro Inoue, Yushi Asadollahi, Reza Sticht, Heinrich Zeilhofer, Hanns Ulrich Rauch, Anita |
| author_role | aut aut aut aut aut aut aut aut aut aut aut aut aut aut aut aut aut |
| author_sort | Begemann, Anaïs |
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| spelling | Begemann, Anaïs Verfasser aut Further corroboration of distinct functional features in SCN2A variants causing intellectual disability or epileptic phenotypes Anaïs Begemann, Mario A. Acuña, Markus Zweier, Marie Vincent, Katharina Steindl, Ruxandra Bachmann-Gagescu, Annette Hackenberg, Lucia Abela, Barbara Plecko, Judith Kroell-Seger, Alessandra Baumer, Kazuhiro Yamakawa, Yushi Inoue, Reza Asadollahi, Heinrich Sticht, Hanns Ulrich Zeilhofer, Anita Rauch Erlangen Friedrich-Alexander-Universität Erlangen-Nürnberg 2019 1 Online-Ressource txt rdacontent c rdamedia cr rdacarrier Archivierung/Langzeitarchivierung gewährleistet DE-101 pdager Nav1.2 Channelopathy Patch-clamp Epilepsy Epileptic encephalopathy Intellectual disability Structural modelling Electrophysiology Acuña, Mario A. Verfasser aut Zweier, Markus Verfasser aut Vincent, Marie Verfasser aut Steindl, Katharina Verfasser aut Bachmann-Gagescu, Ruxandra Verfasser aut Hackenberg, Annette Verfasser aut Abela, Lucia Verfasser aut Plecko, Barbara Verfasser aut Kroell-Seger, Judith Verfasser aut Baumer, Alessandra Verfasser aut Yamakawa, Kazuhiro Verfasser aut Inoue, Yushi Verfasser aut Asadollahi, Reza Verfasser aut Sticht, Heinrich Verfasser aut Zeilhofer, Hanns Ulrich Verfasser aut Rauch, Anita Verfasser aut Sonderdruck aus Molecular Medicine Vol. 25 (2019) 10.1186/s10020-019-0073-6 https://nbn-resolving.org/urn:nbn:de:bvb:29-opus4-107100 Resolving-System kostenfrei Volltext http://d-nb.info/1181428939/34 Langzeitarchivierung Nationalbibliothek kostenfrei Volltext https://open.fau.de/handle/openfau/10710 Verlag kostenfrei Volltext |
| spellingShingle | Begemann, Anaïs Acuña, Mario A. Zweier, Markus Vincent, Marie Steindl, Katharina Bachmann-Gagescu, Ruxandra Hackenberg, Annette Abela, Lucia Plecko, Barbara Kroell-Seger, Judith Baumer, Alessandra Yamakawa, Kazuhiro Inoue, Yushi Asadollahi, Reza Sticht, Heinrich Zeilhofer, Hanns Ulrich Rauch, Anita Further corroboration of distinct functional features in SCN2A variants causing intellectual disability or epileptic phenotypes |
| title | Further corroboration of distinct functional features in SCN2A variants causing intellectual disability or epileptic phenotypes |
| title_auth | Further corroboration of distinct functional features in SCN2A variants causing intellectual disability or epileptic phenotypes |
| title_exact_search | Further corroboration of distinct functional features in SCN2A variants causing intellectual disability or epileptic phenotypes |
| title_full | Further corroboration of distinct functional features in SCN2A variants causing intellectual disability or epileptic phenotypes Anaïs Begemann, Mario A. Acuña, Markus Zweier, Marie Vincent, Katharina Steindl, Ruxandra Bachmann-Gagescu, Annette Hackenberg, Lucia Abela, Barbara Plecko, Judith Kroell-Seger, Alessandra Baumer, Kazuhiro Yamakawa, Yushi Inoue, Reza Asadollahi, Heinrich Sticht, Hanns Ulrich Zeilhofer, Anita Rauch |
| title_fullStr | Further corroboration of distinct functional features in SCN2A variants causing intellectual disability or epileptic phenotypes Anaïs Begemann, Mario A. Acuña, Markus Zweier, Marie Vincent, Katharina Steindl, Ruxandra Bachmann-Gagescu, Annette Hackenberg, Lucia Abela, Barbara Plecko, Judith Kroell-Seger, Alessandra Baumer, Kazuhiro Yamakawa, Yushi Inoue, Reza Asadollahi, Heinrich Sticht, Hanns Ulrich Zeilhofer, Anita Rauch |
| title_full_unstemmed | Further corroboration of distinct functional features in SCN2A variants causing intellectual disability or epileptic phenotypes Anaïs Begemann, Mario A. Acuña, Markus Zweier, Marie Vincent, Katharina Steindl, Ruxandra Bachmann-Gagescu, Annette Hackenberg, Lucia Abela, Barbara Plecko, Judith Kroell-Seger, Alessandra Baumer, Kazuhiro Yamakawa, Yushi Inoue, Reza Asadollahi, Heinrich Sticht, Hanns Ulrich Zeilhofer, Anita Rauch |
| title_short | Further corroboration of distinct functional features in SCN2A variants causing intellectual disability or epileptic phenotypes |
| title_sort | further corroboration of distinct functional features in scn2a variants causing intellectual disability or epileptic phenotypes |
| url | https://nbn-resolving.org/urn:nbn:de:bvb:29-opus4-107100 http://d-nb.info/1181428939/34 https://open.fau.de/handle/openfau/10710 |
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