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  • Molecular assay reagents intended to identify mutations in the cartilage oligomeric matrix protein (COMP) gene, located at chromosome 19p13.1, which encodes for an noncollagenous extracellular matrix (ECM) protein. Mutations at this locus have been identified in patients with childhood early-onset multiple epiphyseal dysplasia (MED) and have also been associated with pseudoachondroplasia (PSACH).
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