Mora-Ayestaran, Nerea; Ochoa, Juan-Pablo; Gómez-González, Cristina; Navarro-Peñalver, Marina; Gallego-Delgado, María; Larrañaga-Moreira, José-M; Robles-Mezcua, Ainhoa; Basurte-Elorz, María-Teresa; Rodríguez-Palomares, José-Fernando; Climent-Paya, Vicente; Jiménez-Jaimez, Juan; Mogollon-Jiménez, María-Victoria; García-Granja, Pablo-Elpidio; García-Álvarez, Ana; Peña-Peña, María-Luisa; Álvarez-Barredo, María; Ripoll-Vera, Tomas; Palomino-Doza, Julián; Bayes-Genis, Antoni; Tiron, Coloma; Fernández, Ana-Isabel; Sabater-Molina, María; Toranzo, Inés; Crespo-Leiro, María-G; Doncel-Abad, Victoria; Lacuey-Lecumberri, Gemma; Limeres-Freire, Javier; I; Cabrera-Borrego, Eva; Kounka-Ait-El-Maalem, Zineb; Vilches, Silvia; González-López, Esther; Villacorta, Eduardo; García-Pinilla, José-M; Barriales-Villa, Roberto; Gimeno-Blanes, Juan-Ramón; García-Pavia, Pablo; Domínguez, Fernando
(OXFORD UNIV PRESS, 2025-12-22)
BACKGROUND AND AIMS: Certain genetic forms of dilated cardiomyopathy (DCM) entail a higher arrhythmic risk. It is unknown whether DCM patients with high-risk arrhythmic genotypes also develop more advanced heart failure ...