Persistent URL of this record https://hdl.handle.net/1887/96770
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De novo mutations in ATP1A3 cause alternating hemiplegia of childhood
- All authors
- 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
- Date
- 2012-09-30
- Journal
- Nature Genetics
- Volume
- 44
- Issue
- 9
- Pages
- 1030 - +