Mutations in beta-myosin S2 that cause familial hypertrophic cardiomyopathy 
(FHC) abolish the interaction with the regulatory domain of myosin-binding 
protein-C

Gruen, M.; Gautel, M.

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Mutations in beta-myosin S2 that cause familial hypertrophic cardiomyopathy (FHC) abolish the interaction with the regulatory domain of myosin-binding protein-C

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Gruen, M., & Gautel, M. (1999). Mutations in beta-myosin S2 that cause familial hypertrophic cardiomyopathy (FHC) abolish the interaction with the regulatory domain of myosin-binding protein-C.

Cite as: https://hdl.handle.net/11858/00-001M-0000-0014-413F-E

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