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-Reference-Cited by-同舟云学术

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

Published:1999-02 Issue:3 Volume:286 Page:933-949
ISSN:0022-2836
Container-title:Journal of Molecular Biology
language:en
Short-container-title:Journal of Molecular Biology

Author:

Gruen Mathias,Gautel Mathias

Publisher

Elsevier BV

Subject

Molecular Biology,Structural Biology

Reference70 articles.

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3. Current Protocols in Molecular Biology;Ausubel,1987

4. Heart C-protein is transiently expressed during skeletal muscle development in the embryo, but persists in cultured myogenic cells;Bähler;Dev. Biol.,1985

5. The ultrastructural localization of C-protein, X-protein and H-protein in rabbit muscle;Bennett;J. Muscle Res. Cell Motil.,1986

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