Defective Peroxisome Membrane Synthesis Due To Mutations in Human PEX3 Causes Zellweger Syndrome, Complementation Group G

Lignende værker

• PEX3 Is the Causal Gene Responsible for Peroxisome Membrane Assembly–Defective Zellweger Syndrome of Complementation Group G
  af: Ghaedi, Kamran, et al.
  Udgivet: (2000)
• Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D.
  af: Honsho, M, et al.
  Udgivet: (1998)
• Animal cell mutants represent two complementation groups of peroxisome-defective Zellweger syndrome.
  af: Shimozawa, N, et al.
  Udgivet: (1992)
• Identification of PEX10, the gene defective in complementation group 7 of the peroxisome-biogenesis disorders.
  af: Warren, D S, et al.
  Udgivet: (1998)
• Human PEX1 cloned by functional complementation on a CHO cell mutant is responsible for peroxisome-deficient Zellweger syndrome of complementation group I
  af: Tamura, Shigehiko, et al.
  Udgivet: (1998)