APA (7th ed.) Citation

SK, G., MM, A., N, M., RA, L., RA, S., HG, S., & LR, G. (2026). Whole-exome sequencing identifies matrisomal gene associations in monogenic cerebral small vessel disease. Journal of neurology, 273(8), . https://doi.org/10.1007/s00415-026-14018-2

Chicago Style (17th ed.) Citation

SK, Guyler, Alfayyadh MM, Maksemous N, Lea RA, Smith RA, Sutherland HG, and Griffiths LR. "Whole-exome Sequencing Identifies Matrisomal Gene Associations in Monogenic Cerebral Small Vessel Disease." Journal of Neurology 273, no. 8 (2026). https://doi.org/10.1007/s00415-026-14018-2.

MLA (9th ed.) Citation

SK, Guyler, et al. "Whole-exome Sequencing Identifies Matrisomal Gene Associations in Monogenic Cerebral Small Vessel Disease." Journal of Neurology, vol. 273, no. 8, 2026, https://doi.org/10.1007/s00415-026-14018-2.