Campuzano, O.; Fernandez-Falgueras, A.; Lemus, X.; Sarquella-Brugada, G.; Cesar, S.; Coll, M.; Mates, J.; Arbelo, E.; Jordà , P.; Perez-Serra, A.;
et al. Short QT Syndrome: A Comprehensive Genetic Interpretation and Clinical Translation of Rare Variants. J. Clin. Med. 2019, 8, 1035.
https://doi.org/10.3390/jcm8071035
AMA Style
Campuzano O, Fernandez-Falgueras A, Lemus X, Sarquella-Brugada G, Cesar S, Coll M, Mates J, Arbelo E, Jordà P, Perez-Serra A,
et al. Short QT Syndrome: A Comprehensive Genetic Interpretation and Clinical Translation of Rare Variants. Journal of Clinical Medicine. 2019; 8(7):1035.
https://doi.org/10.3390/jcm8071035
Chicago/Turabian Style
Campuzano, Oscar, Anna Fernandez-Falgueras, Ximena Lemus, Georgia Sarquella-Brugada, Sergi Cesar, Monica Coll, Jesus Mates, Elena Arbelo, Paloma Jordà , Alexandra Perez-Serra,
and et al. 2019. "Short QT Syndrome: A Comprehensive Genetic Interpretation and Clinical Translation of Rare Variants" Journal of Clinical Medicine 8, no. 7: 1035.
https://doi.org/10.3390/jcm8071035
APA Style
Campuzano, O., Fernandez-Falgueras, A., Lemus, X., Sarquella-Brugada, G., Cesar, S., Coll, M., Mates, J., Arbelo, E., Jordà , P., Perez-Serra, A., del Olmo, B., Ferrer-Costa, C., Iglesias, A., Fiol, V., Puigmulé, M., Lopez, L., Pico, F., Brugada, J., & Brugada, R.
(2019). Short QT Syndrome: A Comprehensive Genetic Interpretation and Clinical Translation of Rare Variants. Journal of Clinical Medicine, 8(7), 1035.
https://doi.org/10.3390/jcm8071035
