Lopez-Sainz, Angela; Dominguez, Fernando; Lopes, Luis Rocha; Ochoa, Juan Pablo; Barriales-Villa, Roberto; Climent, Vicente; Linschoten, Marijke; Tiron, Coloma; Chiriatti, Chiara; Marques, Nuno; Rasmussen, Torsten B; Espinosa, María Ángeles; Beinart, Roy; Quarta, Giovanni; Cesar, Sergi; Field, Ella; Garcia-Pinilla, Jose M; Bilinska, Zofia; Muir, Alison R; Roberts, Angharad M; Santas, Enrique; Zorio, Esther; Peña-Peña, Maria Luisa; Navarro, Marina; Fernandez, Adrian; Palomino-Doza, Julian; Azevedo, Olga; Lorenzini, Massimiliano; García-Álvarez, Maria I; Bento, Dina; Jensen, Morten K; Méndez, Irene; Pezzoli, Laura; Sarquella-Brugada, Georgia; Campuzano, Oscar; Gonzalez-Lopez, Esther; Mogensen, Jens; Kaski, Juan Pablo; Arad, Michael; Brugada, Ramon; Asselbergs, Folkert W; Monserrat, Lorenzo; Olivotto, Iacopo; Elliott, Perry M; Garcia-Pavia, Pablo; European Genetic Cardiomyopathies Initiative Investigators
(Elsevier, 2020-07-14)
BACKGROUND: PRKAG2 gene variants cause a syndrome characterized by cardiomyopathy, conduction disease, and ventricular pre-excitation. Only a small number of cases have been reported to date, and the natural history of the ...