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  • Molecular assay reagents intended to identify mutations in the potassium inwardly rectifying channel, subfamily J, member 2 (KCNJ2) gene, located at chromosome 17q23.1-q24.2, that encodes for a protein that may participate in establishing action potential waveform and excitability of neuronal and muscle tissues. Mutations at this locus have been identified in patients with Andersen-Tawil syndrome, short QT syndrome, and familial atrial fibrillation.
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