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...
שמור ב:
| הוצא לאור ב: | Proc Natl Acad Sci U S A |
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| Principais autores: | , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
National Academy of Sciences
1985
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| נושאים: | |
| גישה מקוונת: | 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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