APA (7th ed.) Citation

A, S., S, P., G, T., C, S., Q, P., DEV, P., & DB, A. (2024). Characterizing and predicting ccRCC-causing missense mutations in Von Hippel-Lindau disease. Human molecular genetics, 33(3), 224. https://doi.org/10.1093/hmg/ddad181

Chicago Style (17th ed.) Citation

A, Serghini, Portelli S, Troadec G, Song C, Pan Q, Pires DEV, and Ascher DB. "Characterizing and Predicting CcRCC-causing Missense Mutations in Von Hippel-Lindau Disease." Human Molecular Genetics 33, no. 3 (2024): 224. https://doi.org/10.1093/hmg/ddad181.

MLA (9th ed.) Citation

A, Serghini, et al. "Characterizing and Predicting CcRCC-causing Missense Mutations in Von Hippel-Lindau Disease." Human Molecular Genetics, vol. 33, no. 3, 2024, p. 224, https://doi.org/10.1093/hmg/ddad181.