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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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| Pubblicato in: | Arrhythm Electrophysiol Rev |
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| Autori principali: | , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Radcliffe Cardiology
2016
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| Soggetti: | |
| Accesso online: | 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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