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Research priorities in sarcomeric cardiomyopathies
The clinical variability in patients with sarcomeric cardiomyopathies is striking: a mutation causes cardiomyopathy in one individual, while the identical mutation is harmless in a family member. Moreover, the clinical phenotype varies ranging from asymmetric hypertrophy to severe dilatation of the...
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| Vydáno v: | Cardiovasc Res |
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| Hlavní autoři: | , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Oxford University Press
2015
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4375392/ https://ncbi.nlm.nih.gov/pubmed/25631582 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/cvr/cvv019 |
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