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

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.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-0014-413F-E Version Permalink: https://hdl.handle.net/11858/00-001M-0000-0014-4140-8

Genre: Other

Alternative Title : Journal of Molecular Biology

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Creators:
Gruen, M.¹, Author
Gautel, M.¹, Author

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1external, ou_persistent22

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Dates: Date issued: 1999

Publication Status: Issued

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Identifiers: URI: ://WOS:000078838900023

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