Family-based investigation of the C677T polymorphism of the methylenetetrahydrofolate reductase gene in ischaemic heart disease.

MLA

Spence, Mark S., et al. “Family-Based Investigation of the C677T Polymorphism of the Methylenetetrahydrofolate Reductase Gene in Ischaemic Heart Disease.” Atherosclerosis, vol. 165, no. 2, Dec. 2002, pp. 293–99. EBSCOhost, https://doi.org/10.1016/s0021-9150(02)00239-3.

APA

Spence, M. S., McGlinchey, P. G., Patterson, C. C., Belton, C., Murphy, G., McMaster, D., Fogarty, D. G., Evans, A. E., & McKeown, P. P. (2002). Family-based investigation of the C677T polymorphism of the methylenetetrahydrofolate reductase gene in ischaemic heart disease. Atherosclerosis, 165(2), 293–299. https://doi.org/10.1016/s0021-9150(02)00239-3

Chicago

Spence, Mark S, Paul G McGlinchey, Chris C Patterson, Christine Belton, Gillian Murphy, Dorothy McMaster, Damian G Fogarty, Alun E Evans, and Pascal P McKeown. 2002. “Family-Based Investigation of the C677T Polymorphism of the Methylenetetrahydrofolate Reductase Gene in Ischaemic Heart Disease.” Atherosclerosis 165 (2): 293–99. doi:10.1016/s0021-9150(02)00239-3.