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Creatine Kinase ATP and Phosphocreatine Energy Supply in a Single Kindred of Patients with Hypertrophic Cardiomyopathy
A lethal and extensively characterized familial form of hypertrophic cardiomyopathy (HC) is due to a point mutation (Arg403Gln) in the cardiac β-myosin heavy-chain (MHC) gene. Although this is associated with abnormal energy metabolism and progression to heart failure in an animal model, in vivo car...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3759602/ https://ncbi.nlm.nih.gov/pubmed/23751935 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.amjcard.2013.05.017 |
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