Home > Specialties > IVD Test Reagent/Kits, Molecular Assay, Gene Anomaly, Mutation, NPHS1

IVD Test Reagent/Kits, Molecular Assay, Gene Anomaly, Mutation, NPHS1

Definition : Molecular assay reagents intended to identify mutations in the nephrosis 1, congenital, Finnish type (nephrin) (NPHS1) gene, located at chromosome 19q13.1, which encodes for the protein nephrin that is a kidney glomerular filtration barrier protein. Mutations at this locus have been identified in patients with congenital nephrotic syndrome of the Finnish type.

Entry Terms : "Nephrotic Syndrome Gene Mutation Reagents" , "Congenital Nephrotic Syndrome Gene Mutation Reagents" , "Finnish Type congenital Nephrotic Syndrome Gene Mutation Reagents" , "NPHS1 Gene Mutation Detection Reagents" , "Reagents, Molecular Assay, Gene Anomaly, Mutation, NPHS1"

UMDC code : 24642

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Exocell Inc

Company Type: Parent

Exocell is a life sciences company that provides market-leading products and services for research and development related to the management of diabetes and its complications.

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