De novo mutations in ATP1A3 cause alternating hemiplegia of childhood

Erin L. Heinzen, Kathryn J. Swoboda, Yuki Hitomi, Fiorella Gurrieri, Boukje De Vries, F. Danilo Tiziano, Bertrand Fontaine, Nicole M. Walley, Sinéad Heavin, Eleni Panagiotakaki, Stefania Fiori, Emanuela Abiusi, Lorena Di Pietro, Matthew T. Sweney, Tara M. Newcomb, Louis Viollet, Chad Huff, Lynn B. Jorde, Sandra P. Reyna, Kelley J. MurphyKevin V. Shianna, Curtis E. Gumbs, Latasha Little, Kenneth Silver, Louis J. Ptáček, Joost Haan, Michel D. Ferrari, Ann M. Bye, Geoffrey K. Herkes, Charlotte M. Whitelaw, David Webb, Bryan J. Lynch, Peter Uldall, Mary D. King, Ingrid E. Scheffer, Giovanni Neri, Alexis Arzimanoglou, Arn M J M Van Den Maagdenberg, Sanjay M. Sisodiya, Mohamad A. Mikati, David B. Goldstein, Stephany Koelewijn, Jessica Kamphorst, Marije Geilenkirchen, Nadine Pelzer, Michel Ferrari, Arn Van Den Maagdenberg, Claudio Zucca, Filippo Franchini, Rosaria Vavassori, Melania Giannotta, Giuseppe Gobbi, Tiziana Granata, Nardo Nardocci, Elisa De Grandis, Edvige Veneselli, Michela Stagnaro, Federico Vigevano, Claudia Oechsler, Sophie Nicole, Miriam Ninan, Brian Neville, Friedrich Ebinger, Carmen Fons, Jaume Campistol, David Kemlink, Sona Nevsimalova, Laura Laan, Cacha Peeters-Scholte, Paul Casaer, Giorgio Casari, Guenter Sange, Georg Spiel, Filippo Martinelli Boneschi, Maria Teresa Bassi, Tsveta Schyns, Francis Crawley, Dominique Poncelin

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