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pro vyhledávání: '"Rawan Jannadi"'
Autor:
Robert Lersch, Rawan Jannadi, Leonie Grosse, Matias Wagner, Marius Frederik Schneider, Celina von Stülpnagel, Florian Heinen, Heidrun Potschka, Ingo Borggraefe
Publikováno v:
Neuroscientist, DOI: 10.1177/10738584221088244 (2022)
Dravet syndrome is a severe developmental and epileptic encephalopathy mostly caused by heterozygous mutation of the SCN1A gene encoding the voltage-gated sodium channel α subunit Nav1.1. Multiple seizure types, cognitive deterioration, behavioral d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fedb6918ae9ecf0eaa8d517089c53ed7
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=64795
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=64795
