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pro vyhledávání: '"Lori A. Smith-Mellecker"'
Autor:
Xiuqiong Zhou, YuJaung Kim, Se Hee Kim, George B. Richerson, Eduardo Bravo, Brian K. Gehlbach, Douglas R. Nordli, Linda Laux, Caitlin K. Thirnbeck, Lori A. Smith-Mellecker
Publikováno v:
Journal of Clinical Investigation. 128:1141-1153
Dravet syndrome (DS) is a severe childhood-onset epilepsy commonly due to mutations of the sodium channel gene SCN1A. Patients with DS have a high risk of sudden unexplained death in epilepsy (SUDEP), widely believed to be due to cardiac mechanisms.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f297a099a19336bea06cd0b524586202
https://doi.org/10.1172/jci94999
https://doi.org/10.1172/jci94999
