Home > Specialties > IVD Test Reagent/Kits, Molecular Assay, Gene Anomaly, Mutation, LAMA2

IVD Test Reagent/Kits, Molecular Assay, Gene Anomaly, Mutation, LAMA2

Definition : Molecular assay reagents intended to identify mutations in the laminin, alpha 2 (LAMA2) gene, located at chromosome 6q22-q23, which encodes for merosin or laminin M, a striated muscle-specific basal-lamina-associated protein. Mutations at this locus have been identified in patients with congenital muscular dystrophy.

Entry Terms : "Merosin-Deficient Congenital Muscular Dystrophy Gene Mutation Reagents" , "Congenital Muscular Dystrophy Gene Mutation Reagents" , "Muscular Dystrophy, Merosin-Deficient Gene Mutation Reagents" , "LAMA2 Gene Mutation Detection Reagents" , "IVD Test Reagent/Kits, Molecular Assay, Inborn Disorder, Monogenic, Muscular Dystrophy" , "Reagents, Molecular Assay, Gene Anomaly, Mutation, LAMA2"

UMDC code : 24591

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