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The Role of Cardiac Troponin T Quantity and Function in Cardiac Development and Dilated Cardiomyopathy
BACKGROUND: Hypertrophic (HCM) and dilated (DCM) cardiomyopathies result from sarcomeric protein mutations, including cardiac troponin T (cTnT, TNNT2). We determined whether TNNT2 mutations cause cardiomyopathies by altering cTnT function or quantity; whether the severity of DCM is related to the ra...
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| Main Authors: | , , , , , , , , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2008
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2441440/ https://ncbi.nlm.nih.gov/pubmed/18612386 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0002642 |
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