Peroxisomal disorders: Improved laboratory diagnosis, new defects and the complicated route to treatment-Reference-Cited by-同舟云学术

Peroxisomal disorders: Improved laboratory diagnosis, new defects and the complicated route to treatment

Published:2018-08 Issue: Volume:40 Page:60-69
ISSN:0890-8508
Container-title:Molecular and Cellular Probes
language:en
Short-container-title:Molecular and Cellular Probes

Author:

Wanders Ronald J.A.^ORCID

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology

Reference73 articles.

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3. Severe plasmalogen deficiency in tissues of infants without peroxisomes (Zellweger syndrome);Heymans;Nature,1983

4. Biogenesis of peroxisomes;Lazarow;Annu. Rev. Cell Biol.,1985

5. Acyl-Coa oxidase and hydratase-dehydrogenase, two enzymes of the peroxisomal beta-oxidation system, are synthesized on free polysomes of clofibrate-treated rat liver;Rachubinski;J. Cell Biol.,1984

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