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