IVD Test Reagent/Kits, Molecular Assay, Gene Anomaly, Mutation, SNCA
Definition : Molecular assay reagents intended to identify mutations in the synuclein, alpha (non A4 component of amyloid precursor) (SNCA) gene, located at chromosome 4q22, which encodes for a protein that may integrate presynaptic signaling and membrane transport of dopamine. This inherited genetic mutation has been identified in patients with familial Parkinson's disease.
Entry Terms : "Parkinson Disease Gene Mutation Reagents" , "Familial Parkinson Disease Type 1 Gene Mutation Reagents" , "SNCA Gene Mutation Detection Reagents" , "Reagents, Molecular Assay, Gene Anomaly, Mutation, SNCA"
UMDC code : 24974