De novo mutations in ATP1A3 cause alternating hemiplegia of childhood

by Heinzen, E.L., Swoboda, K.J., Hitomi, Y., Gurrieri, F., Nicole, S., Vries, B. de, Tiziano, F.D., Fontaine, B., Walley, N.M., Heavin, S., Panagiotakaki, E., Fiori, S., Abiusi, E., Pietro, L. di, Sweney, M.T., Newcomb, T.M., Viollet, L., Huff, C., Jorde, L.B., Reyna, S.P., Murphy, K.J., Shianna, K.V., Gumbs, C.E., Little, L., Silver, K., Ptacek, L.J., Haan, J., Ferrari, M.D., Bye, A.M., Herkes, G.K., Whitelaw, C.M., Webb, D., Lynch, B.J., Uldall, P., King, M.D., Scheffer, I.E., Neri, G., Arzimanoglou, A., Maagdenberg, A.M.J.M. van den, Sisodiya, S.M., Mikati, M.A., Goldstein, D.B., European Alternating Hemiplegia, Biobanca Registro Clinico, European Network Res Alternating
Published 2012