KOR

e-Article

Association of ultra-rare coding variants with genetic generalized epilepsy: A case–control whole exome sequencing study
Document Type
Article
Author
Koko, M.Motelow, J.E.Stanley, K.E.Dhindsa, R.S.Bobbili, D.R.May, P.Alldredge, B.K.Allen, A.S.Altmüller, J.Amrom, D.Andermann, E.Auce, P.Avbersek, A.Baulac, S.Bautista, J.F.Becker, F.Bellows, S.T.Berghuis, B.Berkovic, S.F.Bluvstein, J.Boro, A.Bridgers, J.Burgess, R.Caglayan, H.Cascino, G.D.Cavalleri, G.L.Chung, S.-K.Cieuta-Walti, C.Cloutier, V.Consalvo, D.Cossette, P.Crumrine, P.Delanty, N.Depondt, C.Desbiens, R.Devinsky, O.Dlugos, D.Epstein, M.P.Everett, K.Fiol, M.Fountain, N.B.Francis, B.French, J.Freyer, C.Friedman, D.Gambardella, A.Geller, E.B.Girard, S.Glauser, T.Glynn, S.Goldstein, D.B.Gravel, M.Haas, K.Haut, S.R.Heinzen, E.L.Helbig, I.Hildebrand, M.S.Johnson, M.R.Jorgensen, A.Joshi, S.Kanner, A.Kirsch, H.E.Klein, K.M.Knowlton, R.C.Koeleman, B.P.C.Kossoff, E.H.Krause, R.Krenn, M.Kunz, W.S.Kuzniecky, R.Langley, S.R.LeGuern, E.Lehesjoki, A.-E.Lerche, H.Leu, C.Lortie, A.Lowenstein, D.H.Marson, A.G.Mebane, C.Mefford, H.C.Meloche, C.Moreau, C.Motika, P.V.Muhle, H.Møller, R.S.Nabbout, R.Nguyen, D.K.Nikanorova, M.Novotny, E.J.Nürnberg, P.Ottman, R.O’Brien, T.J.Paolicchi, J.M.Parent, J.M.Park, K.Peter, S.Petrou, S.Petrovski, S.Pickrell, W.O.Poduri, A.Radtke, R.A.Rees, M.I.Regan, B.M.Ren, Z.Sadleir, L.G.Sander, J.W.Sander, T.Scheffer, I.E.Schubert, J.Shellhaas, R.A.Sherr, E.H.Shih, J.J.Shinnar, S.Sills, G.J.Singh, R.K.Siren, A.Sirven, J.Sisodiya, S.M.Smith, M.C.Sonsma, A.C.M.Striano, P.Sullivan, J.Thio, L.L.Thomas, R.H.Venkat, A.Vining, E.P.G.Von Allmen, G.K.Wang, Q.Weber, Y.G.Weckhuysen, S.Weisenberg, J.L.Widdess-Walsh, P.Winawer, M.R.Wolking, S.Zara, F.Zimprich, F.
Source
In: Epilepsia. (Epilepsia, March 2022, 63(3):723-735)
Subject
Language
English
ISSN
15281167
00139580