APA (7th ed.) Citation

Shang, L., Shi, W., Xu, Y., Nong, T., Li, X., Li, Z., . . . Xu, H. (2024). A novel compound heterozygous variation in the FKBP10 gene causes Bruck syndrome without congenital contractures: A case report. Heliyon, 10(7), e28680. https://doi.org/10.1016/j.heliyon.2024.e28680

Chicago Style (17th ed.) Citation

Shang, Liyuan, et al. "A Novel Compound Heterozygous Variation in the FKBP10 Gene Causes Bruck Syndrome Without Congenital Contractures: A Case Report." Heliyon 10, no. 7 (2024): e28680. https://doi.org/10.1016/j.heliyon.2024.e28680.

MLA (9th ed.) Citation

Shang, Liyuan, et al. "A Novel Compound Heterozygous Variation in the FKBP10 Gene Causes Bruck Syndrome Without Congenital Contractures: A Case Report." Heliyon, vol. 10, no. 7, 2024, p. e28680, https://doi.org/10.1016/j.heliyon.2024.e28680.