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  • Molecular assay reagents intended to identify deletions or duplications of the troponin C1, slow skeletal and cardiac type (TNNC1) gene, located at chromosome 3p21.1, which encodes the protein troponin C, slow skeletal and cardiac muscles. Genetic variants at this locus have been associated with dilated cardiomyopathy and familial hypertrophic cardiomyopathy.
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