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

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

Definition : Molecular assay reagents intended to identify mutations in the prosaposin (PSAP) gene, located at chromosome 10q21-q22, which encodes for a protein involved in multiple biologic functions of the nervous and reproductive systems. This genetic mutation has been identified in patients with variants of (i.e., atypical) Gaucher's disease and metachromatic leukodystrophy; mutations are also present in complex sphingolipidosis with fatal infantile glycogen storage disorder.

Entry Terms : "Sphingolipidosis Gene Mutation Reagents" , "Complex Spingolipidosis/Fatal Infantile Storage Disorder Gene Mutation Reagents" , "Leukodystrophy Gene Mutation Reagents" , "Metachromatic Leukodystrophy Gene Mutation Reagents" , "Atypical Gaucher Disease Gene Mutation Reagents" , "PSAP Gene Mutation Detection Reagents" , "Reagents, Molecular Assay, Gene Anomaly, Mutation, PSAP"

UMDC code : 24925

Filters
Manufacturers
Distributors
U.S.companies only
Suppress Subsidiary Companies
   

1-1 of 1 Match(es).

Mayo Medical Laboratories

Company Type: Parent

1-1 of 1 Match(es).

 

Medical Product Guide Optometric Management Product Guide