Neuronal mechanisms of mutations in SCN8A causing epilepsy or intellectual disability

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Neuronal mechanisms of mutations in SCN8A causing epilepsy or intellectual disability

Author: Liu, Yuanyuan; Schubert, Julian; Sonnenberg, Lukas; Helbig, Katherine L.; Hoei-Hansen, Christina E.; Koko, Mahmoud; Rannap, Maert; Lauxmann, Stephan; Huq, Mahbubul; Schneider, Michael C.; Johannesen, Katrine M.; Kurlemann, Gerhard; Gardella, Elena; Becker, Felicitas; Weber, Yvonne G.; Benda, Jan; Moller, Rikke S.; Lerche, Holger
Tübinger Autor(en):
Liu, Yuanyuan
Schubert, Julian
Sonnenberg, Lukas
Koko, Mahmoud
Rannap, Maert
Lauxmann, Stephan
Becker, Felicitas
Weber, Yvonne G.
Benda, Jan
Lerche, Holger
Published in: Brain (2019), Bd. 142, S. 376-390
Verlagsangabe: Oxford Univ Press
Language: English
Full text: http://dx.doi.org/10.1093/brain/awy326
ISSN: 1460-2156
DDC Classifikation: 570 - Life sciences; biology
610 - Medicine and health
Dokumentart: Article
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