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Multi-scale computational models of familial hypertrophic cardiomyopathy: genotype to phenotype
Familial hypertrophic cardiomyopathy (FHC) is an inherited disorder affecting roughly one in 500 people. Its hallmark is abnormal thickening of the ventricular wall, leading to serious complications that include heart failure and sudden cardiac death. Treatment is complicated by variation in the sev...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The Royal Society
2011
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3177620/ https://ncbi.nlm.nih.gov/pubmed/21831889 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1098/rsif.2011.0184 |
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