Identification of PEX10, the gene defective in complementation group 7 of the peroxisome-biogenesis disorders.

Lignende værker

• PEX13 is mutated in complementation group 13 of the peroxisome-biogenesis disorders.
  af: Liu, Y, et al.
  Udgivet: (1999)
• Alternative Splicing Suggests Extended Function of PEX26 in Peroxisome Biogenesis
  af: Weller, Sabine, et al.
  Udgivet: (2005)
• Phenotype-genotype relationships in complementation group 3 of the peroxisome-biogenesis disorders.
  af: Chang, C C, et al.
  Udgivet: (1998)
• Phenotype-genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interaction.
  af: Tamura, S, et al.
  Udgivet: (2001)
• The Peroxisome Biogenesis Factors Pex4p, Pex22p, Pex1p, and Pex6p Act in the Terminal Steps of Peroxisomal Matrix Protein Import
  af: Collins, Cynthia S., et al.
  Udgivet: (2000)