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Heterogeneous Phenotype of Long QT Syndrome Caused by the KCNH2-H562R Mutation: Importance of Familial Genetic Testing.
Muñoz-Esparza C, García-Molina E, Salar-Alcaraz M, Peñafiel-Verdú P, Sánchez-Muñoz JJ, Martínez Sánchez J, Cabañas-Perianes V, Valdés Chávarri M, García Alberola A, Gimeno-Blanes JR. Muñoz-Esparza C, et al. Rev Esp Cardiol (Engl Ed). 2015 Oct;68(10):861-8. doi: 10.1016/j.rec.2014.10.022. Epub 2015 Mar 26. Rev Esp Cardiol (Engl Ed). 2015. PMID: 25819988
The TBX1 Transcription Factor in Cardiac Remodeling After Myocardial Infarction.
Sánchez-Más J, Lax A, Asensio-López MC, Fernández-Del Palacio MJ, Caballero L, Navarro-Peñalver M, Pérez-Martínez MT, Gimeno-Blanes JR, Pascual-Figal DA. Sánchez-Más J, et al. Rev Esp Cardiol (Engl Ed). 2016 Nov;69(11):1042-1050. doi: 10.1016/j.rec.2016.04.033. Epub 2016 Jul 12. Rev Esp Cardiol (Engl Ed). 2016. PMID: 27422448 English, Spanish.
Mutation in JPH2 cause dilated cardiomyopathy.
Sabater-Molina M, Navarro M, García-Molina Sáez E, Garrido I, Pascual-Figal D, González Carrillo J, Gimeno Blanes JR. Sabater-Molina M, et al. Clin Genet. 2016 Nov;90(5):468-469. doi: 10.1111/cge.12825. Epub 2016 Jul 29. Clin Genet. 2016. PMID: 27471098 No abstract available.
71 results