Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D.

Podobne zapisy

• PEX3 Is the Causal Gene Responsible for Peroxisome Membrane Assembly–Defective Zellweger Syndrome of Complementation Group G
  od: Ghaedi, Kamran, i wsp.
  Wydane: (2000)
• Human PEX1 cloned by functional complementation on a CHO cell mutant is responsible for peroxisome-deficient Zellweger syndrome of complementation group I
  od: Tamura, Shigehiko, i wsp.
  Wydane: (1998)
• Phenotype-genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interaction.
  od: Tamura, S, i wsp.
  Wydane: (2001)
• Animal cell mutants represent two complementation groups of peroxisome-defective Zellweger syndrome.
  od: Shimozawa, N, i wsp.
  Wydane: (1992)
• Standardization of complementation grouping of peroxisome-deficient disorders and the second Zellweger patient with peroxisomal assembly factor-1 (PAF-1) defect.
  od: Shimozawa, N, i wsp.
  Wydane: (1993)