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Ultra-rare genetic variation in common epilepsies: a case-control sequencing study von Allen, AS, Bellows, ST, Berkovic, SF, Bridgers, J, Burgess, R, Cavalleri, G, Chung, S-K, Cossette, P, Delanty, N, Dlugos, D, Epstein, MP, Freyer, C, Goldstein, DB, Heinzen, EL, Hildebrand, MS, Johnson, MR, Kuzniecky, R, Lowenstein, DH, Marson, AG, Mayeux, R, Mebane, C, Mefford, HC, O'Brien, TJ, Ottman, R, Petrou, S, Petrovski, S, Pickrell, WO, Poduri, A, Radtke, RA, Rees, MI, Regan, BM, Ren, Z, Scheffer, IE, Sills, GJ, Thomas, RH, Wang, Q, Abou-Khalil, B, Alldredge, BK, Amrom, D, Andermann, E, Andermann, F, Bautista, JF, Bluvstein, J, Boro, A, Cascino, GD, Consalvo, D, Crumrine, P, Devinsky, O, Fiol, M, Fountain, NB, French, J, Friedman, D, Geller, EB, Glauser, T, Glynn, S, Haas, K, Haut, SR, Hayward, J, Helmers, SL, Joshi, S, Kanner, A, Kirsch, HE, Knowlton, RC, Kossoff, EH, Kuperman, R, Motika, PV, Novotny, EJ, Paolicchi, JM, Parent, JM, Park, K, Sadleir, LG, Shellhaas, RA, Sherr, EH, Shih, JJ, Shinnar, S, Singh, RK, Sirven, J, Smith, MC, Sullivan, J, Thio, LL, Venkat, A, Vining, EPG, Von Allmen, GK, Weisenberg, JL, Widdess-Walsh, P, Winawer, MR
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