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  • Molecular assay reagents intended to identify deletions or duplications of the transthyretin (TTR) gene, located at chromosome 18q12.1, which encodes the protein transthyretin. Genetic variants at this locus have been associated with dystransthyretinemic euthyroidal hyperthyroxinemia, amyloidogenic transthyretin amyloidosis, and carpal tunnel syndrome.
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