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  • Molecular assay reagents intended to identify mutations in the glutaryl-coenzyme A dehydrogenase (GCDH) gene, located at chromosome 19p13.2, which provides instructions for the protein glutaryl-CoA dehydrogenase, formed in the mitochondria. Mutations at this locus have been identified in patients with early-onset neonatal glutaricaciduria type I (GA1).
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