Home > Specialties > IVD Test Reagent/Kits, Molecular Assay, Gene Anomaly, Mutation, SPG3A

IVD Test Reagent/Kits, Molecular Assay, Gene Anomaly, Mutation, SPG3A

Definition : Molecular assay reagents intended to identify mutations in the spastic paraplegia 3A, atlastin (SPG3A) gene, located at chromosome 14q22.1, which encodes for a protein that may be involved in axonal maintenance. This inherited genetic mutation has been identified in patients with spastic paraplegia type 3A.

Entry Terms : "Hereditary Spastic Paraplegia Type 3 Gene Mutation Reagents" , "Hereditary Spastic Paraplegia Gene Mutation Reagents" , "Hereditary Spastic Paraparesis Gene Mutation Reagents" , "Familial Spastic Paraplegia Gene Mutation Reagents" , "SPG3A Gene Mutation Detection Reagents" , "Reagents, Molecular Assay, Gene Anomaly, Mutation, SPG3A"

UMDC code : 24978

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