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Actin-associated proteins and cardiomyopathy—the ‘unknown’ beyond troponin and tropomyosin
It has been known for several decades that mutations in genes that encode for proteins involved in the control of actomyosin interactions such as the troponin complex, tropomyosin and MYBP-C and thus regulate contraction can lead to hereditary hypertrophic cardiomyopathy. In recent years, it has bec...
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Springer Berlin Heidelberg
2018
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6082317/ https://www.ncbi.nlm.nih.gov/pubmed/29869751 http://dx.doi.org/10.1007/s12551-018-0428-1 |