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alternating hemiplegia of childhood
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ATP1A3
A protein-protein interaction network for human inherited ataxias and disorders of Purkinje cell degeneration
The phenotypic spectrum of rapid-onset dystonia-parkinsonism (RDP) and mutations in the ATP1A3 gene
ATP1A2
A novel mutation in the ATP1A2 gene causes alternating hemiplegia of childhood
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Endocrine and other factor-regulated calcium reabsorption
Homo sapiens (human)
2 genes
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