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  • Molecular assay reagents intended to identify mutations in the potassium inwardly rectifying channel, subfamily J, member 11 (KCNJ11) gene, located at chromosome 11p15.1, which encodes for a protein that an is integral membrane protein and inward-rectifier type potassium channel. Mutations at this locus have been identified in patients with familial persistent hyperinsulinemic hypoglycemia of infancy (PHHI).
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