Cite

    Shi, M., Leng, X., Li, Y., Chen, Z., Cao, Y., Chung, T., Ip, B. Y., Ip, V. H., Soo, Y. O., Fan, F. S., Ma, S. H., Ma, K., Chan, A. Y. Y., Au, L. W., Leung, H., Lau, A. Y., Mok, V. C., Choy, K. W., Dong, Z., & Leung, T. W. (2022). genome sequencing reveals the role of rare genomic variants in Chinese patients with symptomatic intracranial atherosclerotic disease. Stroke and vascular neurology, 7(3), 182–189. http://access.bl.uk/ark:/81055/vdc_100158007991.0x00000c