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Isogenic models of hypertrophic cardiomyopathy unveil differential phenotypes and mechanism-driven therapeutics
BACKGROUND: Hypertrophic cardiomyopathy (HCM) is a prevalent and complex cardiovascular condition. Despite being strongly associated with genetic alterations, wide variation of disease penetrance, expressivity and hallmarks of progression complicate treatment. We aimed to characterize different huma...
Tallennettuna:
| Julkaisussa: | J Mol Cell Cardiol |
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| Päätekijät: | , , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Academic Press
2020
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7487780/ https://ncbi.nlm.nih.gov/pubmed/32531470 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.yjmcc.2020.06.003 |
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