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- W2096012638 abstract "It has long been noted that while patients with familial hypertrophic cardiomyopathy due to cardiac troponin T (cTnT) mutations often suffer sudden cardiac death, they do not develop significant ventricular hypertrophy, suggesting that a distinct cellular mechanism apart from alterations in myocardial contractility is responsible. A new study has revealed that a single missense mutation in cTnT causes a striking disruption to energy metabolism, leading to cardiomyopathy." @default.
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- W2096012638 date "2003-09-01" @default.
- W2096012638 modified "2023-10-16" @default.
- W2096012638 title "Cardiac troponin T and familial hypertrophic cardiomyopathy: an energetic affair" @default.
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- W2096012638 doi "https://doi.org/10.1172/jci19632" @default.
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