Mutations in filamin-C (FLNC) are involved in the pathogenesis of arrhythmogenic cardiomyopathy (ACM) and dilated cardiomyopathy (DCM), and have been associated with a left ventricular (LV) phenotype, characterized by non-ischemic LV fibrosis, ventricular arrhythmias and sudden cardiac death (SCD).

Filamin C variant-associated Cardiomyopathy: A Pooled Analysis of Individual Patient Data to Evaluate the Clinical Profile and Risk of Sudden Cardiac Death

Celeghin, Rudy;Cipriani, Alberto;Bariani, Riccardo;Bueno Marinas, Maria;Cason, Marco;Bevilacqua, Michela;Gaspari, Monica De;Rizzo, Stefania;Rigato, Ilaria;Pozzo, Stefano Da;Zorzi, Alessandro;Marra, Martina Perazzolo;Thiene, Gaetano;Iliceto, Sabino;Basso, Cristina;Corrado, Domenico;Pilichou, Kalliopi;Bauce, Barbara
2021

Abstract

Mutations in filamin-C (FLNC) are involved in the pathogenesis of arrhythmogenic cardiomyopathy (ACM) and dilated cardiomyopathy (DCM), and have been associated with a left ventricular (LV) phenotype, characterized by non-ischemic LV fibrosis, ventricular arrhythmias and sudden cardiac death (SCD).
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/11577/3403872
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