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

Definition : Molecular assay reagents intended to identify mutations in the tyrosinase (oculocutaneous albinism IA) (TYR) gene, located at chromosome 11q14-q21, which encodes for a copper-containing oxidase that functions in the formation of pigments such as melanins and other polyphenolic compounds. This inherited genetic mutation has been identified in patients with oculocutaneous albinism (tyrosinase negative) types 1A (OCA1A) or 1B (OCA1B).

Entry Terms : "Albinism Gene Mutation Reagents" , "TYR Gene-Related Oculocutaneous Albinism Gene Mutation Reagents" , "Minimal Pigment Oculocutaneous Albinism Gene Mutation Reagents" , "Oculocutaneous Albinism Type 1B (OCA1B) Gene Mutation Reagents" , "Oculocutaneous Albinism Type 1A (OCA1A) Gene Mutation Reagents" , "Oculocutaneous Albinism Type 1 (OCA1) Gene Mutation Reagents" , "Tyrosinase-Related Oculocutaneous Albinism Gene Mutation Reagents" , "TYR Gene Mutation Detection Reagents" , "Reagents, Molecular Assay, Gene Anomaly, Mutation, TYR"

UMDC code : 25003

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Rowley Biochemical Inc

Company Type: Parent

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