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- W2883604038 abstract "A single genetic culprit giving rise to varied forms of ventricular cardiomyopathy is a well-documented phenomenon and likely arises, at least in part, secondary to a combination of genetic modifiers and environmental factors.1,2 Recent work has begun to implicate cardiomyopathy genes in “lone” atrial fibrillation (AF), suggesting that atrial cardiomyopathy may be a subphenotype of the arrhythmia.3–6 It is conceivable that within certain patients and families, cardiomyopathy gene mutations may preferentially manifest with atrial rather than ventricular phenotypes." @default.
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- W2883604038 date "2018-10-01" @default.
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- W2883604038 title "A large familial pathogenic Plakophilin-2 gene (PKP2) deletion manifesting with sudden cardiac death and lone atrial fibrillation: Evidence for alternating atrial and ventricular phenotypes" @default.
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- W2883604038 doi "https://doi.org/10.1016/j.hrcr.2018.07.009" @default.
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