Vatta, Matteo

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Journal Article

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

Cheng, Jianding; Van Norstrand, David W.; Medeiros Domingo, Argelia; Valdivia, Carmen; Tan, Bi-hua; Ye, Bin; Kroboth, Stacie; Vatta, Matteo; Tester, David J.; January, Craig T.; Makielski, Jonathan C.; Ackerman, Michael J. (2009). Alpha1-syntrophin mutations identified in sudden infant death syndrome cause an increase in late cardiac sodium current. Circulation. Arrhythmia and electrophysiology, 2(6), pp. 667-676. Lippincott Williams & Wilkins 10.1161/CIRCEP.109.891440

Ueda, Kazuo; Valdivia, Carmen; Medeiros Domingo, Argelia; Tester, David J.; Vatta, Matteo; Farrugia, Gianrico; Ackerman, Michael J.; Makielski, Jonathan C. (2008). Syntrophin mutation associated with long QT syndrome through activation of the nNOS-SCN5A macromolecular complex. Proceedings of the National Academy of Sciences of the United States of America - PNAS, 105(27), pp. 9355-9360. National Academy of Sciences NAS 10.1073/pnas.0801294105

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