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

Definition : Molecular assay reagents intended to identify mutations in the prion protein (PRNP) gene, located at chromosome 20pter-p12, which encodes for the prion protein that has been implicated in various types of transmissible neurodegenerative spongiform encephalopathies. This genetic mutation has been identified in patients with genetically transmitted prion diseases such as familial Creutzfeldt-Jakob disease (fCJD), Gerstmann-Straussler-Scheinker (GSS) syndrome, and fatal familial insomnia (FFI).

Entry Terms : "Fatal Familial Insomnia (FFI) Gene Mutation Reagents" , "Gerstmann-Strausler-Scheinker (GSS) Syndrome Gene Mutation Reagents" , "Familial Creutzfeld-Jakob Disease (FCJD) Gene Mutation Reagents" , "Creutzfeld-Jakob Disease Gene Mutation Reagents" , "Prion Diseases Gene Mutation Reagents" , "PRNP Gene Mutation Detection Reagents" , "Reagents, Molecular Assay, Gene Anomaly, Mutation, PRNP"

UMDC code : 24919

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