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Cholesterol biosynthesis, peroxisomes and peroxisomal disorders: mevalonate kinase is not only deficient in Zellweger syndrome but also in rhizomelic chondrodysplasia punctata.

AuthorsR J Wanders, G J Romeijn
JournalJournal of inherited metabolic disease (J Inherit Metab Dis) Vol. 21 Issue 3 Pg. 309-12 (Jun 1998) ISSN: 0141-8955 [Print] United States
PMID9686383 (Publication Type: Journal Article)
Chemical References
  • Cholesterol
  • Phosphotransferases (Alcohol Group Acceptor)
  • mevalonate kinase
Topics
  • Cells, Cultured
  • Cholesterol (biosynthesis)
  • Chondrodysplasia Punctata, Rhizomelic (enzymology)
  • Fibroblasts (enzymology)
  • Humans
  • Microbodies
  • Peroxisomal Disorders (enzymology)
  • Phosphotransferases (Alcohol Group Acceptor) (deficiency)
  • Zellweger Syndrome (enzymology)

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