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  • Molecular assay reagents intended to identify deletions or duplications of the ATPase Na+/K+ transporting subunit alpha 2 (ATP1A2) gene, located at chromosome 1q23.2, which encodes the alpha-2 subunit of the sodium/potassium-transporting ATPase. Genetic variants at this locus have been associated with alternating hemiplegia of childhood 1 and familial hemiplegic migraine type 2.
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