Home > Specialties > IVD Test Reagent/Kits, Molecular Assay, Gene Anomaly, Mutation, SCN5A

IVD Test Reagent/Kits, Molecular Assay, Gene Anomaly, Mutation, SCN5A

Definition : Molecular assay reagents intended to identify mutations in the sodium channel, voltage-gated, type V, alpha subunit (SCN5A) gene, located at chromosome 3p21, which encodes for a protein that encodes the alpha subunit of a voltage-gated sodium channel found primarily in cardiac muscle. This inherited genetic mutation has been identified in patients with Brugada (long QT syndrome 3) syndrome and Romano-Ward syndrome (RWS).

Entry Terms : "Long QT Syndrome Type 3 (LQTS3) Gene Mutation Reagents" , "Sudden Infant Death Syndrome (SIDS) Gene Mutation Reagents" , "Sudden Unexpected Nocturnal Death Syndrome Gene Mutation Reagents" , "Brugada Syndrome Gene Mutation Reagents" , "Romano-Ward Syndrome (RWS) Gene Mutation Reagents" , "SCN5A Gene Mutation Detection Reagents" , "Reagents, Molecular Assay, Gene Anomaly, Mutation, SCN5A"

UMDC code : 24951

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Mayo Medical Laboratories

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