Human PEX1 cloned by functional complementation on a CHO cell mutant is responsible for peroxisome-deficient Zellweger syndrome of complementation group I

Ítems similars

• PEX12, the Pathogenic Gene of Group III Zellweger Syndrome: cDNA Cloning by Functional Complementation on a CHO Cell Mutant, Patient Analysis, and Characterization of Pex12p
  per: Okumoto, Kanji, 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)
• Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D.
  per: Honsho, M, et al.
  Publicat: (1998)
• Human PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assembly
  per: Matsuzono, Yuji, et al.
  Publicat: (1999)
• The Peroxin Pex3p Initiates Membrane Assembly in Peroxisome Biogenesis
  per: Ghaedi, Kamran, et al.
  Publicat: (2000)