Exome sequencing of ATP1A3-negative cases of alternating hemiplegia of childhood reveals SCN2A as a novel causative gene

Eleni Panagiotakaki, Francesco Danilo Tiziano, Mohamad A. Mikati, Lisanne S. Vijfhuizen, Sophie Nicole5, Gaetan Lesca, Emanuela Abiusi, Agnese Novelli, Lorena Di Pietro, I. B. AHC Consortium, IAHCRC Consortium, Aster V. E. Harder, Nicole M. Walley, Elisa De Grandis, Anne-Lise Poulat, Vincent Des Portes, Anne Lépine, Marie-Cecile Nassogne, Alexis Arzimanoglou, Rosaria VavassoriJan Koenderink, Christopher H. Thompson, Alfred L. George Jr, Fiorella Gurrieri, Arn M. J. M. van den Maagdenberg, Erin L. Heinzen

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Biochemistry, Genetics and Molecular Biology