Zamani, A. G.Simsek, L.Caksen, H.Yildirim, M. S.2024-02-232024-02-2320191018-48131476-5438https://hdl.handle.net/20.500.12452/1733351st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG) -- JUN 16-19, 2018 -- Milan, ITALY[Abstract Not Availabe]eninfo:eu-repo/semantics/closedAccess[Keyword Not Available]A novel variation in SCN2A gene in a patient with Dravet syndromeConference Object27971971Q1WOS:000489313107219Q2