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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Kaydedildi:
Detaylı Bibliyografya
Yayımlandı:Arrhythm Electrophysiol Rev
Asıl Yazarlar: Akdis, Deniz, Brunckhorst, Corinna, Duru, Firat, Saguner, Ardan M
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Radcliffe Cardiology 2016
Konular:
Clinical Arrhythmias
Online Erişim: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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