APA (7th ed.) Citation

M, S., X, L., Y, L., Z, C., Y, C., T, C., . . . TW, L. (2022). Genome sequencing reveals the role of rare genomic variants in Chinese patients with symptomatic intracranial atherosclerotic disease. Stroke and vascular neurology, 7(3), 182. https://doi.org/10.1136/svn-2021-001157

Chicago Style (17th ed.) Citation

M, Shi, et al. "Genome Sequencing Reveals the Role of Rare Genomic Variants in Chinese Patients with Symptomatic Intracranial Atherosclerotic Disease." Stroke and Vascular Neurology 7, no. 3 (2022): 182. https://doi.org/10.1136/svn-2021-001157.

MLA (9th ed.) Citation

M, Shi, et al. "Genome Sequencing Reveals the Role of Rare Genomic Variants in Chinese Patients with Symptomatic Intracranial Atherosclerotic Disease." Stroke and Vascular Neurology, vol. 7, no. 3, 2022, p. 182, https://doi.org/10.1136/svn-2021-001157.