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The diagnosis of hypertrophic cardiomyopathy by cardiovascular magnetic resonance
Hypertrophic cardiomyopathy (HCM) is the most common genetic disease of the heart. HCM is characterized by a wide range of clinical expression, ranging from asymptomatic mutation carriers to sudden cardiac death as the first manifestation of the disease. Over 1000 mutations have been identified, cla...
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| Hauptverfasser: | , , , , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
BioMed Central
2012
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3309929/ https://ncbi.nlm.nih.gov/pubmed/22348519 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1532-429X-14-17 |
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