IVD Test Reagent/Kits, Molecular Assay, Gene Anomaly, Mutation, RYR2
Definition : Molecular assay reagents intended to identify mutations in the ryanodine receptor 2 (cardiac) (RYR2) gene, located at chromosome 1q42.1-q43, which encodes for a receptor found in cardiac muscle. The encoded protein is one of the components of a calcium channel. This genetic mutation has been identified in patients with arrhythmogenic right ventricular dysplasia 2.
Entry Terms : "Arrhythmogenic Right Ventricular Dysplasia (ARVD) Gene Mutation Reagents" , "Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) Gene Mutation Reagents" , "RYR2-Related Catecholaminergic Ventricular Tachycardia Gene Mutation Reagents" , "Catecholamine-Induced Polymorphic Ventricular Tachycardia (CPVT) Gene Mutation Reagents" , "Familial Polymorphic Ventricular tachycardia (FPVT) Gene Mutation Reagents" , "RYR2 Gene Mutation Detection Reagens" , "Reagents, Molecular Assay, Gene Anomaly, Mutation, RYR2"
UMDC code : 24947