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HARVARD Citation
Shi, M. et al. (2022). Genome sequencing reveals the role of rare genomic variants in Chinese patients with symptomatic intracranial atherosclerotic disease. Stroke and vascular neurology. 7 (3), pp. 182-189. [Online].
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Shi, M. et al. (2022). Genome sequencing reveals the role of rare genomic variants in Chinese patients with symptomatic intracranial atherosclerotic disease. Stroke and vascular neurology. 7 (3), pp. 182-189. [Online].