Pathogenic cardiomyopathy gene variants inform prognosis in atrial fibrillation: results from exome sequencing in over 17,000 patients in TIMI trials

Abstract Background Rare genetic variants in cardiomyopathy genes are associated with risk of atrial fibrillation (AF), even in the absence of overt ventricular dysfunction. Data on clinical outcomes for rare genetic variant carriers among patients with AF remain sparse. Purpose We aimed to study th...

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Veröffentlicht in:	European heart journal 2024-10, Vol.45 (Supplement_1)
Hauptverfasser:	Jurgens, S, Melloni, G E M, Kany, S, Berg, D D, Bonaca, M P, Giugliano, R P, Wiviott, S D, Bhatt, D L, Steg, P G, Raz, I, Pirruccello, J P, Sabatine, M S, Marston, N A, Ellinor, P T, Ruff, C T
Format:	Artikel
Sprache:	eng
Online-Zugang:	Volltext
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