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

Eleni Panagiotakaki, Francesco D. Tiziano, Mohamad A. Mikati, Lisanne S. Vijfhuizen, Sophie Nicole, Gaetan Lesca, Emanuela Abiusi, Agnese Novelli, Lorena Di Pietro, Aster V.E. Harder, Nicole M. Walley, Elisa De Grandis, Anne Lise Poulat, Vincent Des Portes, Anne Lépine, Marie Cecile Nassogne, Alexis Arzimanoglou, Rosaria Vavassori, Jan Koenderink, Christopher H. ThompsonAlfred L. George, Fiorella Gurrieri, Arn M.J.M. van den Maagdenberg*, Erin L. Heinzen*

*Corresponding author for this work

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Biochemistry, Genetics and Molecular Biology

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