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Revista Espanola De Cardiologia|May 2, 2009
A homozygous MYBPC3 gene mutation associated with a severe phenotype and a high risk of sudden death in a family with hypertrophic cardiomyopathyMartín F Ortiz, María Isabel Rodríguez-García, Manuel Hermida-Prieto, et al.
Revista Espanola De Cardiologia|August 27, 2010
Severe cardiac conduction disturbances and pacemaker implantation in patients with hypertrophic cardiomyopathyRoberto Barriales-Villa, Raúl Centurión-Inda, Xusto Fernández-Fernández, et al.
Journal of the American College of Cardiology|December 3, 2016
Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic CardiomyopathiesMartín F Ortiz-Genga, Sofía Cuenca, Matteo Dal Ferro, et al.
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