Case Report: A Novel NKX2-5 Mutation in a Family With Congenital Heart Defects, Left Ventricular Non-compaction, Conduction Disease, and Sudden Cardiac Death by Paula Morlanes-Gracia, Guido Antoniutti, Jorge Alvarez-Rubio, Jorge Alvarez-Rubio, Laura Torres-Juan, Laura Torres-Juan, Damian Heine-Suñer, Damian Heine-Suñer, Tomás Ripoll-Vera, Tomás Ripoll-Vera, Tomás Ripoll-Vera

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Genotype-Phenotype Correlation in Hypertrophic Cardiomyopathy: New Variant p.Arg652Lys in <i>MYH7</i> by Guido Antoniutti, Fiama Giuliana Caimi-Martinez, Jorge Álvarez-Rubio, Paula Morlanes-Gracia, Jaume Pons-Llinares, Blanca Rodríguez-Picón, Elena Fortuny-Frau, Laura Torres-Juan, Damian Heine-Suner, Tomas Ripoll-Vera

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New Variant in Placophilin-2 Gene Causing Arrhythmogenic Myocardiopathy by Fiama Caimi-Martinez, Guido Antoniutti, Rocio Blanco, Bernardo García de la Villa, Nelson Alvarenga, Nancy Govea-Callizo, Laura Torres-Juan, Damián Heine-Suñer, Jordi Rosell-Andreo, David Crémer Luengos, Jorge Alvarez-Rubio, Tomás Ripoll-Vera

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