APA (7th ed.) Citation

T, B., I, K., S, K., C, K., SJ, M., KM, J., . . . D, L. (2026). Gene Portals: A Framework for Integrating Clinical, Functional, and Structural Evidence into Rare Disease Variant Classification. MedRxiv : the preprint server for health sciences. https://doi.org/10.64898/2026.03.05.26347086

Chicago Style (17th ed.) Citation

T, Brünger, et al. "Gene Portals: A Framework for Integrating Clinical, Functional, and Structural Evidence into Rare Disease Variant Classification." MedRxiv : The Preprint Server for Health Sciences 2026. https://doi.org/10.64898/2026.03.05.26347086.

MLA (9th ed.) Citation

T, Brünger, et al. "Gene Portals: A Framework for Integrating Clinical, Functional, and Structural Evidence into Rare Disease Variant Classification." MedRxiv : The Preprint Server for Health Sciences, 2026, https://doi.org/10.64898/2026.03.05.26347086.