Standardization of complementation grouping of peroxisome-deficient disorders and the second Zellweger patient with peroxisomal assembly factor-1 (PAF-1) defect.

Eitemau Tebyg

• Animal cell mutants represent two complementation groups of peroxisome-defective Zellweger syndrome.
  gan: Shimozawa, N, et al.
  Cyhoeddwyd: (1992)
• PEX3 Is the Causal Gene Responsible for Peroxisome Membrane Assembly–Defective Zellweger Syndrome of Complementation Group G
  gan: Ghaedi, Kamran, et al.
  Cyhoeddwyd: (2000)
• Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D.
  gan: Honsho, M, et al.
  Cyhoeddwyd: (1998)
• Human PEX1 cloned by functional complementation on a CHO cell mutant is responsible for peroxisome-deficient Zellweger syndrome of complementation group I
  gan: Tamura, Shigehiko, et al.
  Cyhoeddwyd: (1998)
• Human PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assembly
  gan: Matsuzono, Yuji, et al.
  Cyhoeddwyd: (1999)