Animal cell mutants represent two complementation groups of peroxisome-defective Zellweger syndrome.

Ítems similars

• Standardization of complementation grouping of peroxisome-deficient disorders and the second Zellweger patient with peroxisomal assembly factor-1 (PAF-1) defect.
  per: Shimozawa, N, et al.
  Publicat: (1993)
• Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D.
  per: Honsho, M, et al.
  Publicat: (1998)
• PEX3 Is the Causal Gene Responsible for Peroxisome Membrane Assembly–Defective Zellweger Syndrome of Complementation Group G
  per: Ghaedi, Kamran, et al.
  Publicat: (2000)
• Human PEX1 cloned by functional complementation on a CHO cell mutant is responsible for peroxisome-deficient Zellweger syndrome of complementation group I
  per: Tamura, Shigehiko, et al.
  Publicat: (1998)
• Temperature-sensitive phenotypes of peroxisome-assembly processes represent the milder forms of human peroxisome-biogenesis disorders.
  per: Imamura, A, et al.
  Publicat: (1998)