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 AlıntıVeltmann, 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 AlıntıVeltmann, 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.
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