Why the study?
Myosin binding protein C accounts for ~ 40% of all known mutations in hypertrophic cardiomyopathy, warranting a complete understanding of its molecular function in the cardiac sarcomere.
Design
Review
Authors
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Offers mechanistic context for MyBP-C mutations in HCM; leaves targeted therapy development open pending clinical validation.
Key points are not available for this paper at this time.
Heling et al. (2020) studied this question.
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