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  • Molecular assay reagents intended to identify deletions or duplications of the ATP binding cassette subfamily C member 8 (ABCC8) gene, located at chromosome 11p15.1, which encodes the protein ATP-binding cassette sub-family C member 8. Genetic variants at this locus have been associated with transient neonatal diabetes mellitus 2, permanent neonatal diabetes mellitus, persistent hyperinsulinemic hypoglycemia of infancy, leucine-induced hypoglycemia, and diabetes mellitus type 2.
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