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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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Bibliografski detalji
Glavni autori: Campbell, Stuart G., McCulloch, Andrew D.
Format: Artigo
Jezik:Inglês
Izdano: The Royal Society 2011
Teme:
Online pristup: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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