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  • Molecular assay reagents intended to identify deletions and duplications in the huntingtin (HTT) gene, located at chromosome 4p16.3, which encodes the huntington disease protein. Genetic alterations in the HTT gene have been associated with Huntington\'s disease. While the vast majority of pathogenic HTT mutations involve expansions of CAG trinucleotide repeats, these reagents may be used to analyze the HTT gene for deletions or duplications in patients with Huntington-like symptoms lacking CAG repeat expansion.
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