Identification of Rare Genetic Variants in Familial Spontaneous Coronary Artery Dissection and Evidence for Shared Biological Pathways.

MLA

Turley, Tamiel N., et al. “Identification of Rare Genetic Variants in Familial Spontaneous Coronary Artery Dissection and Evidence for Shared Biological Pathways.” Journal of Cardiovascular Development & Disease (JCDD), vol. 10, no. 9, Sept. 2023, p. 393. EBSCOhost, https://doi.org/10.3390/jcdd10090393.

APA

Turley, T. N., Theis, J. L., Evans, J. M., Fogarty, Z. C., Gulati, R., Hayes, S. N., Tweet, M. S., & Olson, T. M. (2023). Identification of Rare Genetic Variants in Familial Spontaneous Coronary Artery Dissection and Evidence for Shared Biological Pathways. Journal of Cardiovascular Development & Disease (JCDD), 10(9), 393. https://doi.org/10.3390/jcdd10090393

Chicago

Turley, Tamiel N., Jeanne L. Theis, Jared M. Evans, Zachary C. Fogarty, Rajiv Gulati, Sharonne N. Hayes, Marysia S. Tweet, and Timothy M. Olson. 2023. “Identification of Rare Genetic Variants in Familial Spontaneous Coronary Artery Dissection and Evidence for Shared Biological Pathways.” Journal of Cardiovascular Development & Disease (JCDD) 10 (9): 393. doi:10.3390/jcdd10090393.