A novel homozygous frameshift mutation in the APOA1 gene associated with marked high-density lipoprotein deficiency.

MLA

Takeda, Tadashi, et al. “A Novel Homozygous Frameshift Mutation in the APOA1 Gene Associated with Marked High-Density Lipoprotein Deficiency.” Journal of Clinical Lipidology, vol. 16, no. 4, July 2022, pp. 423–33. EBSCOhost, https://doi.org/10.1016/j.jacl.2022.06.001.

APA

Takeda, T., Ide, T., Okuda, D., Kuroda, M., Asada, S., Kirinashizawa, M., Yamamoto, M., Miyoshi, J., Yokote, K., & Mizutani, N. (2022). A novel homozygous frameshift mutation in the APOA1 gene associated with marked high-density lipoprotein deficiency. Journal of Clinical Lipidology, 16(4), 423–433. https://doi.org/10.1016/j.jacl.2022.06.001

Chicago

Takeda, Tadashi, Tsubasa Ide, Daishi Okuda, Masayuki Kuroda, Sakiyo Asada, Mika Kirinashizawa, Misato Yamamoto, Junko Miyoshi, Koutaro Yokote, and Naohiro Mizutani. 2022. “A Novel Homozygous Frameshift Mutation in the APOA1 Gene Associated with Marked High-Density Lipoprotein Deficiency.” Journal of Clinical Lipidology 16 (4): 423–33. doi:10.1016/j.jacl.2022.06.001.