IVD Test Reagent/Kits, Molecular Assay, Gene Anomaly, Mutation, KCNJ2
Definition : 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.
Entry Terms : "Andersen-Tawil Syndrome Gene Mutation Reagents" , "Andersen Syndrome Gene Mutation Reagents" , "Long QT Syndrome-7 (LQT7) Gene Mutation Reagents" , "KCNJ2 Gene Mutation Detection Reagents" , "Reagents, Molecular Assay, Gene Anomaly, Mutation, KCNJ2"
UMDC code : 24582