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The genetics of hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy (HCM) is most commonly transmitted as an autosomal dominant trait, caused by mutations in genes encoding cardiac sarcomere proteins(1–3). Other inheritable causes of the disease include mutations in genes coding for proteins important in calcium handling or that form part...
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| 發表在: | Glob Cardiol Sci Pract |
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| Main Authors: | , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Magdi Yacoub Heart Foundation
2018
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6209452/ https://ncbi.nlm.nih.gov/pubmed/30393648 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.21542/gcsp.2018.36 |
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