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Arrhythmogenic Cardiomyopathy: Electrical and Structural Phenotypes
This overview gives an update on the molecular mechanisms, clinical manifestations, diagnosis and therapy of arrhythmogenic cardiomyopathy (ACM). ACM is mostly hereditary and associated with mutations in genes encoding proteins of the intercalated disc. Three subtypes have been proposed: the classic...
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| Vydáno v: | Arrhythm Electrophysiol Rev |
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| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Radcliffe Cardiology
2016
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5013177/ https://ncbi.nlm.nih.gov/pubmed/27617087 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.15420/AER.2016.4.3 |
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