08:48 02/05/2025
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Nguồn tham khảo
  1. Pingitore, P., Pirazzi, C., Mancina, R. M., Motta, B. M., Indiveri, C., Pujia, A., Montalcini, T., Hedfalk, K., & Romeo, S. (2014). Recombinant PNPLA3 protein shows triglyceride hydrolase activity and its I148M mutation results in loss of function. Biochimica Et Biophysica Acta (BBA) – Molecular and Cell Biology of Lipids, 1841(4), 574–580. https://doi.org/10.1016/j.bbalip.2013.12.006
  2. Luo, F., Oldoni, F., & Das, A. (2021). TM6SF2: a novel genetic player in nonalcoholic fatty liver and cardiovascular disease. Hepatology Communications, 6(3), 448–460. https://doi.org/10.1002/hep4.1822
  3. Varadharajan, V., Massey, W., & Brown, J. M. (2022). Membrane-bound O-acyltransferase 7 (MBOAT7)-driven phosphatidylinositol remodeling in advanced liver disease. Journal of Lipid Research, 63(7), 100234. https://doi.org/10.1016/j.jlr.2022.100234
  4. French, M. (2023, July 7). Fatty liver: Is it hereditary? https://www.medicalnewstoday.com/articles/is-fatty-liver-hereditary#other-causes
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