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Risk Stratification in Hypertrophic Cardiomyopathy
Hypertrophic cardiomyopathy (HCM) is a hereditary primary myocardial disease that is most commonly due to mutations within genes encoding sarcomeric contractile proteins and is characterised by left ventricular hypertrophy in the absence of a cardiac or systemic cause. Although the overall prognosis...
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| Publicat a: | Eur Cardiol |
|---|---|
| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Radcliffe Cardiology
2015
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6159455/ https://ncbi.nlm.nih.gov/pubmed/30310420 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.15420/ecr.2015.10.01.31 |
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