APA Alıntı

Veltmann, C., Barajas‐Martinez, H., Wolpert, C., Borggrefe, M., Schimpf, R., Pfeiffer, R., . . . Hu, D. (2016). Further Insights in the Most Common SCN5A Mutation Causing Overlapping Phenotype of Long QT Syndrome, Brugada Syndrome, and Conduction Defect. J Am Heart Assoc.

Chicago Stili Alıntı

Veltmann, Christian, et al. "Further Insights in the Most Common SCN5A Mutation Causing Overlapping Phenotype of Long QT Syndrome, Brugada Syndrome, and Conduction Defect." J Am Heart Assoc 2016.

MLA Alıntı

Veltmann, Christian, et al. "Further Insights in the Most Common SCN5A Mutation Causing Overlapping Phenotype of Long QT Syndrome, Brugada Syndrome, and Conduction Defect." J Am Heart Assoc 2016.