APA (7th ed.) Citation

Havndrup, O., Bundgaard, H., Andersen, P. S., Larsen, L. A., Vuust, J., Kjeldsen, K., & Christiansen, M. (2001). The Val606Met mutation in the cardiac beta-myosin heavy chain gene in patients with familial hypertrophic cardiomyopathy is associated with a high risk of sudden death at young age. American Journal of Cardiology, 87(11), 1315. https://doi.org/10.1016/s0002-9149(01)01532-6

Chicago Style (17th ed.) Citation

Havndrup, O., H. Bundgaard, P S. Andersen, L A. Larsen, J. Vuust, K. Kjeldsen, and M. Christiansen. "The Val606Met Mutation in the Cardiac Beta-myosin Heavy Chain Gene in Patients with Familial Hypertrophic Cardiomyopathy Is Associated with a High Risk of Sudden Death at Young Age." American Journal of Cardiology 87, no. 11 (2001): 1315. https://doi.org/10.1016/s0002-9149(01)01532-6.

MLA (9th ed.) Citation

Havndrup, O., et al. "The Val606Met Mutation in the Cardiac Beta-myosin Heavy Chain Gene in Patients with Familial Hypertrophic Cardiomyopathy Is Associated with a High Risk of Sudden Death at Young Age." American Journal of Cardiology, vol. 87, no. 11, 2001, p. 1315, https://doi.org/10.1016/s0002-9149(01)01532-6.