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Delineation of Molecular Pathways Involved in Cardiomyopathies Caused by Troponin T Mutations
Familial hypertrophic cardiomyopathy (FHC) is associated with mild to severe cardiac problems and is the leading cause of sudden death in young people and athletes. Although the genetic basis for FHC is well-established, the molecular mechanisms that ultimately lead to cardiac dysfunction are not we...
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| Publicat a: | Mol Cell Proteomics |
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| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
The American Society for Biochemistry and Molecular Biology
2016
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5083082/ https://ncbi.nlm.nih.gov/pubmed/27022107 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/mcp.M115.057380 |
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