Home > Specialties > Reagents, Molecular Assay, Gene Anomaly, Mutation, SLC26A4

Reagents, Molecular Assay, Gene Anomaly, Mutation, SLC26A4

Definition : Molecular assay reagents intended to identify mutations in the solute carrier family 26, member 4 (SLC26A4) gene, located at chromosome 7q31, which encodes for a transport protein that is a sodium-independent transporter of chloride and iodide and is active in the thyroid, kidney, and inner ear. This inherited genetic mutation has been identified in patients with nonsyndromic deafness.

Entry Terms : "Neurosensory Hearing Impairment Gene Mutation Reagents" , "Pendred Syndrome Gene Mutation Reagents" , "Congenital Deafness Type 4 Gene Mutation Reagents" , "Deafness Gene Mutation Reagents" , "SLC26A4 Gene Mutation Detection Reagents"

UMDC code : 24971

   

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