Items where Author is "Begemann, Anaïs"
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Article
Asadollahi, Reza
ORCID: 0000-0002-1497-0564
, Delvendahl, Igor, Muff, Rebecca, Tan, Ge, Rodríguez, Daymé González, Turan, Soeren, Russo, Martina, Oneda, Beatrice, Joset, Pascal, Boonsawat, Paranchai, Masood, Rahim, Mocera, Martina, Ivanovski, Ivan, Baumer, Alessandra, Bachmann-Gagescu, Ruxandra, Schlapbach, Ralph, Rehrauer, Hubert, Steindl, Katharina, Begemann, Anaïs, Reis, André, Winkler, Jürgen, Winner, Beate, Müller, Martin and Rauch, Anita
(2023)
Pathogenic SCN2A variants cause early-stage dysfunction in patient-derived neurons.
Human Molecular Genetics, 32 (13).
pp. 2192-2204.
ISSN 0964-6906 (Print), 1460-2083 (Online)
(doi:https://doi.org/10.1093/hmg/ddad048)
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
ORCID: 0000-0002-1497-0564
, Sticht, Heinrich, Zeilhofer, Hanns Ulrich and Rauch, Anita
(2019)
Further corroboration of distinct functional features in SCN2A variants causing intellectual disability or epileptic phenotypes.
Molecular Medicine, 25 (1).
ISSN 1076-1551 (Print), 1528-3658 (Online)
(doi:https://doi.org/10.1186/s10020-019-0073-6)