APA (7th ed.) Citation

Kim, K. Y., Heo, Y. J., Ko, J. M., Lee, Y. A., Shin, C. H., Ki, C. S., & Lee, Y. J. (2024). Familial chylomicronemia syndrome: Case reports of siblings with deletions of the GPIHBP1 gene. BMC Endocrine Disorders, 24(1), 1. https://doi.org/10.1186/s12902-024-01574-9

Chicago Style (17th ed.) Citation

Kim, Ka Young, You Joung Heo, Jung Min Ko, Young Ah Lee, Choong Ho Shin, Chang Seok Ki, and Yun Jeong Lee. "Familial Chylomicronemia Syndrome: Case Reports of Siblings with Deletions of the GPIHBP1 Gene." BMC Endocrine Disorders 24, no. 1 (2024): 1. https://doi.org/10.1186/s12902-024-01574-9.

MLA (9th ed.) Citation

Kim, Ka Young, et al. "Familial Chylomicronemia Syndrome: Case Reports of Siblings with Deletions of the GPIHBP1 Gene." BMC Endocrine Disorders, vol. 24, no. 1, 2024, p. 1, https://doi.org/10.1186/s12902-024-01574-9.