De novo mutations in ATP1A3 cause alternating hemiplegia of childhood
- Author(s):
- 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. (0000-0001-9691-9449); 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 (0000-0002-9310-5535); Sisodiya, S.M.; Mikati, M.A.; Goldstein, D.B.; European Alternating Hemiplegia; Biobanca Registro Clinico; European Network Res Alternating
- Published
- 2012
- Publication type
- Article / Letter to editor
- Date issued
- 2012-09-30
- Language
- English
- Is part of
- Nature Genetics (2012), Vol. 44, no. 9, p. 1030-+
- hdl
- 1887/96770
- doi
- 10.1038/ng.2358