TY - JOUR AU - Akhtar, Mohammed Majid AU - Lorenzini, Massimiliano AU - Cicerchia, Marcos AU - Ochoa, Juan Pablo AU - Hey, Thomas Morris AU - Sabater Molina, Maria AU - Restrepo-Cordoba, Maria Alejandra AU - Dal Ferro, Matteo AU - Stolfo, Davide AU - Johnson, Renee AU - Larrañaga-Moreira, José M AU - Robles-Mezcua, Ainhoa AU - Rodriguez-Palomares, Jose F AU - Casas, Guillem AU - Peña-Peña, Maria Luisa AU - Lopes, Luis Rocha AU - Gallego-Delgado, Maria AU - Franaszczyk, Maria AU - Laucey, Gemma AU - Rangel-Sousa, Diego AU - Basurte, Mayte AU - Palomino-Doza, Julian AU - Villacorta, Eduardo AU - Bilinska, Zofia AU - Limeres Freire, Javier AU - Garcia Pinilla, José M AU - Barriales-Villa, Roberto AU - Fatkin, Diane AU - Sinagra, Gianfranco AU - Garcia-Pavia, Pablo AU - Gimeno, Juan R AU - Mogensen, Jens AU - Monserrat, Lorenzo AU - Elliott, Perry M PY - 2020 DO - 10.1161/CIRCHEARTFAILURE.119.006832 UR - http://hdl.handle.net/10668/16299 T2 - Circulation. Heart failure AB - Truncating variants in the TTN gene (TTNtv) are the commonest cause of heritable dilated cardiomyopathy. This study aimed to study the phenotypes and outcomes of TTNtv carriers. Five hundred thirty-seven individuals (61% men; 317 probands) with TTNtv... LA - en KW - cardiomyopathy, dilated KW - connectin KW - heart failure KW - phenotype KW - sex KW - Adult KW - Aged KW - Aged, 80 and over KW - Arrhythmias, Cardiac KW - Cardiomyopathy, Dilated KW - Connectin KW - Europe KW - Female KW - Genetic Predisposition to Disease KW - Genetic Variation KW - Heart Failure KW - Humans KW - Longitudinal Studies KW - Male KW - Middle Aged KW - New South Wales KW - Phenotype KW - Prognosis KW - Risk Assessment KW - Risk Factors KW - Sex Factors KW - Stroke Volume KW - Time Factors KW - Ventricular Dysfunction, Left KW - Ventricular Function, Left KW - Ventricular Remodeling TI - Clinical Phenotypes and Prognosis of Dilated Cardiomyopathy Caused by Truncating Variants in the TTN Gene. TY - research article VL - 13 ER -