Kölker, S., Gleich, F., Mütze, U., & Opladen, T. (2022). Rare disease registries are key to evidence-based personalized medicine: Highlighting the european experience. Frontiers in endocrinology, 13, .
Chicago Style (17th ed.) CitationKölker, Stefan, Florian Gleich, Ulrike Mütze, and Thomas Opladen. "Rare Disease Registries Are Key to Evidence-based Personalized Medicine: Highlighting the European Experience." Frontiers in Endocrinology 13 (2022).
MLA (9th ed.) CitationKölker, Stefan, et al. "Rare Disease Registries Are Key to Evidence-based Personalized Medicine: Highlighting the European Experience." Frontiers in Endocrinology, vol. 13, 2022.
Warning: These citations may not always be 100% accurate.