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Yin, Liheng; Zahradnikova, Alexandra; Rizzetto, Riccardo; Boncompagni, Simona; Rabesahala de Meritens, Camille; Zhang, Yadan; Joanne, Pierre; Marqués-Sulé, Elena; Aguilar-Sánchez, Yuriana; Fernández-Tenorio, Miguel; Villejoubert, Olivier; Li, Linwei; Wang, Yue Yi; Mateo, Philippe; Nicolas, Valérie; Gerbaud, Pascale; Lai, F. Anthony; Perrier, Romain; Álvarez, Julio L.; Niggli, Ernst; ... (2021). Impaired Binding to Junctophilin-2 and Nanostructural Alteration in CPVT Mutation. Circulation research, 129(3), e35-e52. American Heart Association 10.1161/CIRCRESAHA.121.319094
Medeiros Domingo, Argelia; Valdivia, Carmen R. (2014). Disease Caused by Mutations in NaV-β Subunit Genes. Cardiac Electrophysiology Clinics, 6(4), pp. 785-795. WB Saunders 10.1016/j.ccep.2014.08.008
Cheng, Jianding; Van Norstrand, David W.; Medeiros Domingo, Argelia; Tester, David J.; Valdivia, Carmen R.; Tan, Bi-Hua; Vatta, Matteo; Makielski, Jonathan C.; Ackerman, Michael J. (2011). LQTS-associated mutation A257G in α1-syntrophin interacts with the intragenic variant P74L to modify its biophysical phenotype. Cardiogenetics, 1(1) PAGEPress
Valdivia, Carmen R.; Medeiros Domingo, Argelia; Ye, Bin; Shen, Win-Kuang; Algiers, Timothy J.; Ackerman, Michael J.; Makielski, Jonathan C. (2010). Loss-of-function mutation of the SCN3B-encoded sodium channel {beta}3 subunit associated with a case of idiopathic ventricular fibrillation. Cardiovascular research, 86(3), pp. 392-400. Oxford University Press 10.1093/cvr/cvp417
Tan, Bi-Hua; Pundi, Kavitha N.; Van Norstrand, David W; Valdivia, Carmen R.; Tester, David J.; Medeiros Domingo, Argelia; Makielski, Jonathan C.; Ackerman, Michael J. (2010). Sudden infant death syndrome-associated mutations in the sodium channel beta subunits. Heart rhythm, 7(6), pp. 771-778. Elsevier 10.1016/j.hrthm.2010.01.032
Tan, Bi-Hua; Iturralde-Torres, Pedro; Medeiros Domingo, Argelia; Nava, Santiago; Tester, David J.; Valdivia, Carmen R.; Tusié-Luna, Teresa; Ackerman, Michael J.; Makielski, Jonathan C. (2007). A novel C-terminal truncation SCN5A mutation from a patient with sick sinus syndrome, conduction disorder and ventricular tachycardia. Cardiovascular research, 76(3), pp. 409-417. Oxford University Press 10.1016/j.cardiores.2007.08.006
