PEX3 Is the Causal Gene Responsible for Peroxisome Membrane Assembly–Defective Zellweger Syndrome of Complementation Group G

Antzeko izenburuak

• Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D.
  nork: Honsho, M, et al.
  Argitaratua: (1998)
• Human PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assembly
  nork: Matsuzono, Yuji, et al.
  Argitaratua: (1999)
• Human PEX1 cloned by functional complementation on a CHO cell mutant is responsible for peroxisome-deficient Zellweger syndrome of complementation group I
  nork: Tamura, Shigehiko, et al.
  Argitaratua: (1998)
• 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
  nork: Okumoto, Kanji, et al.
  Argitaratua: (1998)
• Mutations in Novel Peroxin Gene PEX26 That Cause Peroxisome-Biogenesis Disorders of Complementation Group 8 Provide a Genotype-Phenotype Correlation
  nork: Matsumoto, Naomi, et al.
  Argitaratua: (2003)