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Paper Details

Phenotypic Expression, Natural History, and Risk Stratification of Cardiomyopathy Caused by Filamin C Truncating Variants.
Circulation
39
2021
Cardiomyopathy, D, D/HT, DSP, DSP-related arrhythmogenic cardiomyopathies, FLNCtv, Filamin C, Filamin C Truncating Variants, Filamin C truncating variants, HT, LMNA, LVAD, arrhythmias, arrhythmogenic cardiomyopathy, arrhythmogenic left dominant cardiomyopathy, arrhythmogenic right ventricular cardiomyopathy, dilated cardiomyopathy, end, genetic cardiomyopathies, heart failure, left ventricular dysfunction, men, nonarrhythmic death, patients, right, sudden cardiac death, ventricular arrhythmias
Author NameAffiliation
Diane FatkinVictor Chang Cardiac Research Institute, and St Vincent's Clinical School
Diane FatkinSt Vincent's Hospital
Cynthia A JamesThe Johns Hopkins University
Victoria N ParikhStanford Center for Inherited Cardiovascular Disease
Euan A AshleyStanford Center for Inherited Cardiovascular Disease
Matthew R G TaylorCardiovascular Institute and Adult Medical Genetics Program, University of Colorado Anschutz Medical Campus
Luisa MestroniCardiovascular Institute and Adult Medical Genetics Program, University of Colorado Anschutz Medical Campus
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