Cite
Reinvestigation of Peroxisomal 3-Ketoacyl-CoA Thiolase Deficiency: Identification of the True Defect at the Level of D-Bifunctional Protein.
MLA
Ferdinandusse, S., et al. “Reinvestigation of Peroxisomal 3-Ketoacyl-CoA Thiolase Deficiency: Identification of the True Defect at the Level of D-Bifunctional Protein.” American Journal of Human Genetics, vol. 70, no. 6, June 2002, p. 1589. EBSCOhost, https://doi.org/10.1086/340970.
APA
Ferdinandusse, S., van Grunsven, E. G., Oostheim, W., Denis, S., Hogenhout, E. M., Ijlst, L., van Roermund, C. W. T., Waterham, H. R., Goldfischer, S., & Wanders, R. J. A. (2002). Reinvestigation of Peroxisomal 3-Ketoacyl-CoA Thiolase Deficiency: Identification of the True Defect at the Level of D-Bifunctional Protein. American Journal of Human Genetics, 70(6), 1589. https://doi.org/10.1086/340970
Chicago
Ferdinandusse, S., E. G. van Grunsven, W. Oostheim, S. Denis, E. M. Hogenhout, L. Ijlst, C. W. T. van Roermund, H. R. Waterham, S. Goldfischer, and R. J. A. Wanders. 2002. “Reinvestigation of Peroxisomal 3-Ketoacyl-CoA Thiolase Deficiency: Identification of the True Defect at the Level of D-Bifunctional Protein.” American Journal of Human Genetics 70 (6): 1589. doi:10.1086/340970.