APA (7th ed.) Citation

R, L., D, Z., C, L., Y, C., Y, B., N, Z., . . . E, H. (2025). Characterization of a novel SCN5A mutation associated with long QT syndrome and arrhythmogenic right ventricular cardiomyopathy in a family. Forensic science, medicine, and pathology, 21(1), 33. https://doi.org/10.1007/s12024-024-00863-y

Chicago Style (17th ed.) Citation

R, Li, et al. "Characterization of a Novel SCN5A Mutation Associated with Long QT Syndrome and Arrhythmogenic Right Ventricular Cardiomyopathy in a Family." Forensic Science, Medicine, and Pathology 21, no. 1 (2025): 33. https://doi.org/10.1007/s12024-024-00863-y.

MLA (9th ed.) Citation

R, Li, et al. "Characterization of a Novel SCN5A Mutation Associated with Long QT Syndrome and Arrhythmogenic Right Ventricular Cardiomyopathy in a Family." Forensic Science, Medicine, and Pathology, vol. 21, no. 1, 2025, p. 33, https://doi.org/10.1007/s12024-024-00863-y.