Mutations in β-myosin S2 that cause familial hypertrophic cardiomyopathy (FHC) abolish the interaction with the regulatory domain of myosin-binding protein-C 1 1Edited by J. Karn

Mathias Gruen, Mathias Gautel

Journal of Molecular Biology · 1999 · 243 citations · 65 references

Concepts

References

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