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

Definition : Molecular assay reagents intended to identify mutations in the patched homologue (PTCH) gene, located at chromosome 9q22.3, which encodes for a protein implicated in the formation of embryonic structures and in tumorigenesis and that functions as a tumor suppressor. This genetic mutation has been identified in patients with holoprosencephaly-7 and nevoid basal cell carcinoma syndrome (NBCSS), also known as Gorlin's syndrome.

Entry Terms : "Gorlin Syndrome Gene Mutation Reagents" , "Nevoid Basal Cell Carcinoma Syndrome (NBCCS) Gene Mutation Reagents" , "Basal Cell Carcinoma Gene Mutation Reagents" , "Basal Cell Nevus Syndrome Gene Mutation Reagents" , "Holoprosencephaly 7 Gene Mutation Reagents" , "PTCH Gene Mutation Detection REagents" , "Reagents, Molecular Assay, Gene Anomaly, Mutation, PTCH"

UMDC code : 24928

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