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  • Molecular assay reagents intended to identify mutations in the troponin T2, cardiac type (TNNT2) gene, located at chromosome 1q32.1, which encodes the protein troponin T, cardiac muscle. Genetic variants at this locus have been associated with familial restrictive cardiomyopathy, familial hypertrophic cardiomyopathy, left ventricular noncompaction, and primary dilated cardiomyopathy.
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