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Reagents, Molecular Assay, Gene Anomaly, Mutation, SPG20

Definition : Molecular assay reagents intended to identify mutations in the spastic paraplegia 20, spartin (SPG20) gene, located at chromosome 13q13.3, which encodes for a protein that may be involved in endosomal transport, microtubule dynamics, or both. This inherited genetic mutation has been identified in patients with Troyer syndrome (hereditary spastic paraplegia type 20).

Entry Terms : "Hereditary Spastic Paraplegia Type 20 Gene Mutation Reagents" , "Troyer Syndrome Gene Mutation Reagents" , "Hereditary Spastic Paraplegia Gene Mutation Reagents" , "Hereditary Spastic Paraparesis Gene Mutation Reagents" , "Familial Spastic Paraplegia Gene Mutation Reagents" , "SPG20 Gene Mutation Detection Reagents"

UMDC code : 24977

   

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