학술논문
SCN1A overexpression, associated with a genomic region marked by a risk variant for a common epilepsy, raises seizure susceptibility
Document Type
Article
Author
Silvennoinen, K.; Pagni, S.; Martins Custodio, H.; Mills, J.; Sisodiya, S.M.; Gawel, K.; van der Ent, W.; Kirstein-Smardzewska, K.J.; Tiraboschi, E.; Esguerra, C.V.; Tsortouktzidis, D.; Pitsch, J.; van Loo, K.M.J.; Schoch, S.; Becker, A.J.; Alhusaini, S.; Whelan, C.D.; Picardo, R.; Michalak, Z.; Thom, M.; Thompson, P.M.; de Zubicaray, G.I.; McMahon, K.L.; Mudge, J.M.; Frankish, A.; Wright, M.J.
Source
In: Acta Neuropathologica . (Acta Neuropathologica, July 2022, 144(1):107-127)
Subject
Language
English
ISSN
14320533
00016322
00016322