IVD Test Reagent/Kits, Molecular Assay, Gene Anomaly, Mutation, KCNQ1
Definition : Molecular assay reagents intended to identify mutations in the potassium voltage-gated channel, KQT-like subfamily, member 1 (KCNQ1) gene, located at chromosome 11p15.5, which encodes for a protein involved in potassium-channel formation and function and helps move potassium out of the cell. Mutations at this locus have been identified in patients with familial atrial fibrillation, JLNS, Romano-Ward syndrome, and short QT syndromes.
Entry Terms : "Cardioauditory Syndrome of Jervell and Lange-Nielsen Gene Mutation Reagents" , "Long QT Syndrome Type 1 (LQTS1) Gene Mutation Reagents" , "Romano-Ward Syndrome Gene Mutation Reagents" , "Jervell and Lange-Nielsen Syndrome (JLNS) Gene Mutation Reagents" , "KCNQ1 Gene Mutation Detection Reagents" , "Reagents, Molecular Assay, Gene Anomaly, Mutation, KCNQ1"
UMDC code : 24583