IVD Test Reagent/Kits, Molecular Assay, Gene Anomaly, Mutation, KCNE2
Definition : Molecular assay reagents intended to identify mutations in the potassium voltage-gated channel, Isk-related family, member 2 (KCNE2) gene, located at chromosome 21q22.12, which encodes for a protein that regulates the activity of potassium ion channels. Mutations at this locus have been identified in patients with Romano-Ward syndrome and familial atrial fibrillation.
Entry Terms : "Long QT Syndrome Type 6 (LQTS6) Gene Mutation Reagents" , "Romano-Ward Syndrome (RWS) Gene Mutation Reagents" , "Familial Atrial Fibrillation Gene Mutation Reagents" , "KCNE2 Gene Mutation Detection Reagents" , "Reagents, Molecular Assay, Gene Anomaly, Mutation, KCNE2"
UMDC code : 24579