Cite
Genotypic and phenotypic features in homozygous familial hypercholesterolemia caused by proprotein convertase subtilisin/kexin type 9 (PCSK9) gain-of-function mutation.
MLA
Mabuchi, Hiroshi, et al. “Genotypic and Phenotypic Features in Homozygous Familial Hypercholesterolemia Caused by Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9) Gain-of-Function Mutation.” Atherosclerosis, vol. 236, no. 1, Sept. 2014, pp. 54–61. EBSCOhost, https://doi.org/10.1016/j.atherosclerosis.2014.06.005.
APA
Mabuchi, H., Nohara, A., Noguchi, T., Kobayashi, J., Kawashiri, M., Inoue, T., Mori, M., Tada, H., Nakanishi, C., Yagi, K., Yamagishi, M., Ueda, K., Takegoshi, T., Miyamoto, S., Inazu, A., & Koizumi, J. (2014). Genotypic and phenotypic features in homozygous familial hypercholesterolemia caused by proprotein convertase subtilisin/kexin type 9 (PCSK9) gain-of-function mutation. Atherosclerosis, 236(1), 54–61. https://doi.org/10.1016/j.atherosclerosis.2014.06.005
Chicago
Mabuchi, Hiroshi, Atsushi Nohara, Tohru Noguchi, Junji Kobayashi, Masa-aki Kawashiri, Takeshi Inoue, Mika Mori, et al. 2014. “Genotypic and Phenotypic Features in Homozygous Familial Hypercholesterolemia Caused by Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9) Gain-of-Function Mutation.” Atherosclerosis 236 (1): 54–61. doi:10.1016/j.atherosclerosis.2014.06.005.