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Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlation. Citations & References

  • Authors: Matsumoto N, Tamura S, Furuki S, Miyata N, Moser A, Shimozawa N, Moser HW, Suzuki Y, Kondo N, Fujiki Y
  • Journal: Am J Hum Genet (2003) 73:233-246
  • PubMed ID: 12851857

Involvement of the endoplasmic reticulum in peroxisome formation. Citations & References

  • Authors: Geuze HJ, Murk JL, Stroobants AK, Griffith JM, Kleijmeer MJ, Koster AJ, Verkleij AJ, Distel B, Tabak HF
  • Journal: Mol Biol Cell (2003) 14:2900-2907
  • PubMed ID: 12857873
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