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  • Molecular assay reagents intended to identify mutations in the ceroid-lipofuscinosis, neuronal 2 (CLN2) gene, located at chromosome 11p15, which encodes for nonspecific lysosomal peptidase that generates tripeptides. Mutations at this locus have been identified in patients with infantile late-onset neuronal ceroid-lipofuscinoses (NCL) type 2.
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