Liver disease predominates in a mouse model for mild human Zellweger spectrum disorder

Kevin Berendse, Maxim Boek, Marion Gijbels, Nicole N. Van der Wel, Femke C. Klouwer, Marius A. van den Bergh-Weerman, Abhijit Babaji Shinde, Rob Ofman, Bwee Tien Poll-The, Sander M. Houten, Myriam Baes, Ronald J. A. Wanders, Hans R. Waterham*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Original languageEnglish
Pages (from-to)2774-2787
Number of pages14
JournalBiochimica et Biophysica Acta-Molecular Basis of Disease
Volume1865
Issue number10
DOIs
Publication statusPublished - 1 Oct 2019

Keywords

  • Peroxisome biogenesis disorder
  • Peroxisome
  • Metabolism
  • Zellweger syndrome
  • Bile acid synthesis
  • Cholestasis
  • PEROXISOME-BIOGENESIS
  • BETA-OXIDATION
  • CLINICAL-MANIFESTATIONS
  • FATTY-ACIDS
  • MITOCHONDRIAL
  • DIAGNOSIS
  • MICE
  • DYSFUNCTION
  • PATHOLOGY
  • DEFECTS

Cite this

Berendse, K., Boek, M., Gijbels, M., Van der Wel, N. N., Klouwer, F. C., van den Bergh-Weerman, M. A., Shinde, A. B., Ofman, R., Poll-The, B. T., Houten, S. M., Baes, M., Wanders, R. J. A., & Waterham, H. R. (2019). Liver disease predominates in a mouse model for mild human Zellweger spectrum disorder. Biochimica et Biophysica Acta-Molecular Basis of Disease, 1865(10), 2774-2787. https://doi.org/10.1016/j.bbadis.2019.06.013