Home > Specialties > IVD Test Reagent/Kits, Molecular Assay, Gene Anomaly, Mutation, CPT2

IVD Test Reagent/Kits, Molecular Assay, Gene Anomaly, Mutation, CPT2

Definition : Molecular assay reagents intended to identify mutations in the carnitine palmitoyltransferase II (CPT2) gene, located at chromosome 1p32, which encodes for carnitine palmitoyltransferase II that participates in transporting long-chain fatty acids into the mitochondria. Mutations at this locus have been identified in patients with carnitine palmitoyltransferase II (CPT2) deficiency.

Entry Terms : "Carnitine Palmitoyltransferase II (CPT2) Deficiency Gene Mutation Detection Reagents" , "CPT2 Gene Mutation Detection Reagents" , "Reagents, Molecular Assay, Gene Anomaly, Mutation, CPT2"

UMDC code : 24372

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Mayo Medical Laboratories

Company Type: Parent

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