S, S., FF, C., E, F., GB, D., G, D. P., GD, M., . . . A, V. (2026). FBXW7-Related Neurodevelopmental Disorder: Clinical Spectrum, Molecular Mechanisms, and Tumor Predisposition. Human mutation, 2026, 3764750. https://doi.org/10.1155/humu/3764750
Chicago Style (17th ed.) CitationS, Savasta, Comisi FF, Fiumicelli E, Dell'Isola GB, Di Pasquale G, Mangano GD, Zagaroli L, Salpietro V, and Verrotti A. "FBXW7-Related Neurodevelopmental Disorder: Clinical Spectrum, Molecular Mechanisms, and Tumor Predisposition." Human Mutation 2026 (2026): 3764750. https://doi.org/10.1155/humu/3764750.
MLA (9th ed.) CitationS, Savasta, et al. "FBXW7-Related Neurodevelopmental Disorder: Clinical Spectrum, Molecular Mechanisms, and Tumor Predisposition." Human Mutation, vol. 2026, 2026, p. 3764750, https://doi.org/10.1155/humu/3764750.