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. Thompson,Alfred L. George Jr.,Fiorella Gurrieri,Arn M. J. M. van den Maagdenberg,Erin L. Heinzen European Journal of Human Genetics（2024）
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