European Journal of Human Genetics, Published online: 14 December 2023; doi:10.1038/s41431-023-01489-4
Exome sequencing of ATP1A3-negative cases of alternating hemiplegia of childhood reveals SCN2A as a novel causative geneEuropean Journal of Human Genetics, Published online: 14 December 2023; doi:10.1038/s41431-023-01489-4
Exome sequencing of ATP1A3-negative cases of alternating hemiplegia of childhood reveals SCN2A as a novel causative gene