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

Definition : Molecular assay reagents intended to identify mutations in the myelin protein zero (MPZ) gene, located at chromosome 1q22, which encodes for the myelin protein zero made in the Schwann cells. Myelin protein zero is required for the proper formation and maintenance of myelin. Mutations at this locus have been identified in patients with Charcot-Marie-Tooth neuropathy 1B (HMSN Ib).

Entry Terms : "Roussy-Levy Dystasia Gene Mutation Reagents" , "Entrapment Neuropathy Gene Mutation Reagents" , "Familial Recurrent Polyneuropathy Gene Mutation Reagents" , "Dejerine-Sottas Syndrome Gene Mutation Reagents" , "Dejerine Syndrome Gene Mutation Reagents" , "Charcot-Marie-Tooth Neuropathy Type 1 Gene Mutation Reagents" , "Hereditary Neuropathy Gene Mutation Reagents" , "MPZ Gene Mutation Detection Reagents" , "Reagents, Molecular Assay, Gene Anomaly, Mutation, MPZ"

UMDC code : 24611

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