APA (7th ed.) Citation

D, I., S, N., S, M., J, M., H, I., M, S., . . . N, S. (2026). Delineating the Genetic Basis of RNF213-related vasculopathies: The association of PKHD1 variants with bilateral cerebral vasculopathy. European journal of human genetics : EJHG, 34(6), 788. https://doi.org/10.1038/s41431-026-02030-z

Chicago Style (17th ed.) Citation

D, Ishigami, et al. "Delineating the Genetic Basis of RNF213-related Vasculopathies: The Association of PKHD1 Variants with Bilateral Cerebral Vasculopathy." European Journal of Human Genetics : EJHG 34, no. 6 (2026): 788. https://doi.org/10.1038/s41431-026-02030-z.

MLA (9th ed.) Citation

D, Ishigami, et al. "Delineating the Genetic Basis of RNF213-related Vasculopathies: The Association of PKHD1 Variants with Bilateral Cerebral Vasculopathy." European Journal of Human Genetics : EJHG, vol. 34, no. 6, 2026, p. 788, https://doi.org/10.1038/s41431-026-02030-z.