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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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Dettagli Bibliografici
Pubblicato in:Arrhythm Electrophysiol Rev
Autori principali: Akdis, Deniz, Brunckhorst, Corinna, Duru, Firat, Saguner, Ardan M
Natura: Artigo
Lingua:Inglês
Pubblicazione: Radcliffe Cardiology 2016
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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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