ResearcherID Møller, R S, Heron, S E, Larsen, L H G, Lim, C X, Ricos, M G, Bayly, M A, van Kempen, M J A, Klinkenberg, S, Andrews, I, Kelley, K, Ronen, G M, Callen, D, McMahon, J M, Yendle, S C, Carvill, G L, Mefford, H C, Nabbout, R, Poduri, A, Striano, P, Baglietto, M G, Zara, F, Smith, N J, Pridmore, C, Gardella, E, Nikanorova, M, Dahl, H A, Gellert, P, Scheffer, I E, Gunning, B, Kragh-Olsen, B & Dibbens, L M 2015, ' Mutations in KCNT1 cause a spectrum of focal epilepsies ', Epilepsia, vol. 56, no. 9, pp. e114-e120 . https://doi.org/10.1111/epi.13071 Epilepsia, 56(9), E114-E120. Wiley Epilepsia, 56(9), e114. Wiley-Blackwell
Nature genetics 47(1), 39-46 (2014). doi:10.1038/ng.3144 Muona, M, Berkovic, S F, Dibbens, L M, Oliver, K L, Maljevic, S, Bayly, M A, Joensuu, T, Canafoglia, L, Franceschetti, S, Michelucci, R, Markkinen, S, Heron, S E, Hildebrand, M S, Andermann, E, Andermann, F, Gambardella, A, Tinuper, P, Licchetta, L, Scheffer, I E, Criscuolo, C, Filla, A, Ferlazzo, E, Ahmad, J, Ahmad, A, Baykan, B, Said, E, Topcu, M, Riguzzi, P, King, M D, Ozkara, C, Andrade, D M, Engelsen, B A, Crespel, A, Lindenau, M, Lohmann, E, Saletti, V, Massano, J, Privitera, M, Espay, A J, Kauffmann, B, Duchowny, M, Moller, R S, Straussberg, R, Afawi, Z, Ben-Zeev, B, Samocha, K E, Daly, M J, Petrou, S, Lerche, H, Palotie, A & Lehesjoki, A E 2015, ' A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy ', Nature Genetics, vol. 47, no. 1, pp. 39-46 . https://doi.org/10.1038/ng.3144