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Peroxisome biogenesis disorders: Molecular basis for impaired peroxisomal membrane assembly

  • Published:2012-09 Issue:9 Volume:1822 Page:1337-1342
  • ISSN:0925-4439
  • Container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
  • language:en
  • Short-container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease

Author:

Fujiki Yukio,Yagita Yuichi,Matsuzaki Takashi

Funder

Science and Technology Agency of Japan

Grants-in-Aid for Scientific Research

The Ministry of Education, Culture, Sports, Science, and Technology of Japan

Takeda Science Foundation

Japan Foundation for Applied Enzymology

Publisher

Elsevier BV

Subject

Molecular Biology,Molecular Medicine

Reference60 articles.

1. Peroxisomal disorders: the single peroxisomal enzyme deficiencies;Wanders;Biochim. Biophys. Acta,2006

2. The Peroxisome Biogenesis Disorders;Gould,2001

3. Peroxisome biogenesis disorders;Fujiki,2003

4. Mutations in novel peroxin gene PEX26 that cause peroxisome biogenesis disorders of complementation group 8 provide a genotype–phenotype correlation;Matsumoto;Am. J. Hum. Genet.,2003

5. Peroxisome biogenesis disorders;Weller;Annu. Rev. Genomics Hum. Genet.,2003

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