Home > Specialties > IVD Test Reagent/Kits, Molecular Assay, Gene Anomaly, Mutation, KCNH2

IVD Test Reagent/Kits, Molecular Assay, Gene Anomaly, Mutation, KCNH2

Definition : Molecular assay reagents intended to identify mutations in the potassium voltage-gated channel, subfamily H, member 2 (KCNH2) gene, located at chromosome 7q35-q36, which belongs to a family of genes that provide instructions for making potassium channels. Mutations at this locus have been identified in patients with Romano-Ward, short QT syndrome, and are long QT syndrome.

Entry Terms : "Long QT Syndrome Type 2 (LQTS2) Gene Mutation Reagents" , "Romano-Ward Syndrome (RWS) Gene Mutation Reagents" , "Familial Atrial Fibrillation Gene Mutation Reagents" , "KCNH2 Gene Mutation Detection Reagents" , "Reagents, Molecular Assay, Gene Anomaly, Mutation, KCNH2"

UMDC code : 24580

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