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Echocardiographic diagnosis of the different phenotypes of hypertrophic cardiomyopathy
Hypertrophic Cardiomyopathy (HCM) is an inherited cardiovascular disorder of great genetic heterogeneity and has a prevalence of 0.1 – 0.2 % in the general population. Several hundred mutations in more than 27 genes, most of which encode sarcomeric structures, are associated with the HCM phenotype....
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| 出版年: | Cardiovasc Ultrasound |
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| 主要な著者: | , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BioMed Central
2016
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4982201/ https://ncbi.nlm.nih.gov/pubmed/27519172 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12947-016-0072-5 |
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