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Mechanical dysfunction of the sarcomere induced by a pathogenic mutation in troponin T drives cellular adaptation
Familial hypertrophic cardiomyopathy (HCM), a leading cause of sudden cardiac death, is primarily caused by mutations in sarcomeric proteins. The pathogenesis of HCM is complex, with functional changes that span scales, from molecules to tissues. This makes it challenging to deconvolve the biophysic...
| Autores principales: | , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Rockefeller University Press
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8054178/ https://www.ncbi.nlm.nih.gov/pubmed/33856419 http://dx.doi.org/10.1085/jgp.202012787 |