APA (7th ed.) Citation

MM, A., T, Z., N, M., HG, S., RA, L., & LR, G. (2026). Identification of case-specific copy number variants reveals novel genetic insights into familial hemiplegic migraine pathogenesis. Genomics, 118(3), 111245. https://doi.org/10.1016/j.ygeno.2026.111245

Chicago Style (17th ed.) Citation

MM, Alfayyadh, Zielke T, Maksemous N, Sutherland HG, Lea RA, and Griffiths LR. "Identification of Case-specific Copy Number Variants Reveals Novel Genetic Insights into Familial Hemiplegic Migraine Pathogenesis." Genomics 118, no. 3 (2026): 111245. https://doi.org/10.1016/j.ygeno.2026.111245.

MLA (9th ed.) Citation

MM, Alfayyadh, et al. "Identification of Case-specific Copy Number Variants Reveals Novel Genetic Insights into Familial Hemiplegic Migraine Pathogenesis." Genomics, vol. 118, no. 3, 2026, p. 111245, https://doi.org/10.1016/j.ygeno.2026.111245.