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Exome sequencing of ATP1A3-negative cases of alternating hemiplegia of childhood reveals SCN2A as a novel causative gene
CSNK2B: A broad spectrum of neurodevelopmental disability and epilepsy severity
Analysis of shared heritability in common disorders of the brain
Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood-a study of 155 patients
Distinct neurological disorders with ATP1A3 mutations
De novo mutations in ATP1A3 cause alternating hemiplegia of childhood