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  • Molecular assay reagents intended to identify mutations in the propionyl Coenzyme A carboxylase, alpha polypeptide (PCCA) gene, located at chromosome 13q32, which encodes for the alpha subunit of the enzyme propionyl-CoA carboxylase that is involved in the normal processing of proteins. Mutations at this locus have been identified in patients with propionic acidemia and early-onset organic aciduria.
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