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  • Molecular assay reagents intended to identify deletions or duplications of the small nuclear ribonucleoprotein polypeptide N (SNRPN) gene, located at chromosome 15q11.2, which encodes the protein small nuclear ribonucleoprotein-associated protein N. Genetic variants at this locus have been associated with Prader-Willi syndrome and autistic disorder of childhood onset.
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