Romeo, S., Yin, W., Kozlitina, J., Pennacchio, L. A., Boerwinkle, E., Hobbs, H. H., & Cohen, J. C. (2009). Rare loss-of-function mutations in ANGPTL family members contribute to plasma triglyceride levels in humans. The Journal of clinical investigation, 119(1), 70-79. https://doi.org/10.1172/JCI37118
Chicago-Zitierstil (17. Ausg.)Romeo, Stefano, Wu Yin, Julia Kozlitina, Len A. Pennacchio, Eric Boerwinkle, Helen H. Hobbs, und Jonathan C. Cohen. "Rare Loss-of-function Mutations in ANGPTL Family Members Contribute to Plasma Triglyceride Levels in Humans." The Journal of Clinical Investigation 119, no. 1 (2009): 70-79. https://doi.org/10.1172/JCI37118.
MLA-Zitierstil (9. Ausg.)Romeo, Stefano, et al. "Rare Loss-of-function Mutations in ANGPTL Family Members Contribute to Plasma Triglyceride Levels in Humans." The Journal of Clinical Investigation, vol. 119, no. 1, 2009, pp. 70-79, https://doi.org/10.1172/JCI37118.