Peroxisomal organization in normal and cerebrohepatorenal (Zellweger) syndrome fibroblasts.
The reported absence of morphologically detectable peroxisomes in liver and kidney tissue cells from patients affected by the autosomic recessive, inherited metabolic disease known as cerebrohepatorenal, or Zellweger, syndrome was studied in fibroblasts, assuming it to be a generalized defect. Norma...
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| Publicat a: | Proc Natl Acad Sci U S A |
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| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
National Academy of Sciences
1985
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC391248/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2995971/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.82.19.6556 |
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