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Cell models of arrhythmogenic cardiomyopathy: advances and opportunities
Arrhythmogenic cardiomyopathy is a rare genetic disease that is mostly inherited as an autosomal dominant trait. It is associated predominantly with mutations in desmosomal genes and is characterized by the replacement of the ventricular myocardium with fibrous fatty deposits, arrhythmias and a high...
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| Publicat a: | Dis Model Mech |
|---|---|
| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
The Company of Biologists Ltd
2017
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5536909/ https://ncbi.nlm.nih.gov/pubmed/28679668 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dmm.029363 |
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