Home > Specialties > Reagents, Molecular Assay, Gene Anomaly, Mutation, SPG3A

Reagents, 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"

UMDC code : 24978

   

No results at this time.

 

Medical Product Guide Optometric Management Product Guide