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Clinical implications of cardiac troponin T mutations that cause familial hypertrophic cardiomyopathy

Clinical implications of cardiac troponin T mutations that cause familial hypertrophic cardiomyopathy. Circulation. 1994; 90:I-442.


Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.