Genetic basis of peroxisome-assembly mutants of humans, Chinese hamster ovary cells, and yeast: identification of a new complementation group of peroxisome-biogenesis disorders apparently lacking peroxisomal-membrane ghosts

Am J Hum Genet. 1998 Dec;63(6):1898-903. doi: 10.1086/302142.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CHO Cells
  • Cells, Cultured
  • Cricetinae
  • Fibroblasts
  • Genetic Complementation Test
  • Humans
  • Intracellular Membranes / ultrastructure
  • Microbodies / ultrastructure*
  • Mutation*
  • Peroxisomal Disorders / genetics*
  • Peroxisomal Disorders / metabolism
  • Peroxisomal Disorders / pathology
  • Yeasts / genetics
  • Zellweger Syndrome / genetics
  • Zellweger Syndrome / pathology