APA (7th ed.) Citation

Raghavan, N. S., Brickman, A. M., Andrews, H., Manly, J. J., Schupf, N., Lantigua, R., . . . Project, T. A. D. S. (2018). Whole‐exome sequencing in 20,197 persons for rare variants in Alzheimer's disease. Annals of Clinical & Translational Neurology, 5(7), 832. https://doi.org/10.1002/acn3.582

Chicago Style (17th ed.) Citation

Raghavan, Neha S., et al. "Whole‐exome Sequencing in 20,197 Persons for Rare Variants in Alzheimer's Disease." Annals of Clinical & Translational Neurology 5, no. 7 (2018): 832. https://doi.org/10.1002/acn3.582.

MLA (9th ed.) Citation

Raghavan, Neha S., et al. "Whole‐exome Sequencing in 20,197 Persons for Rare Variants in Alzheimer's Disease." Annals of Clinical & Translational Neurology, vol. 5, no. 7, 2018, p. 832, https://doi.org/10.1002/acn3.582.