Complementation study of peroxisome-deficient disorders by immunofluorescence staining and characterization of fused cells
- 1 March 1992
- journal article
- Published by Springer Nature in Human Genetics
- Vol. 88 (5), 491-499
- https://doi.org/10.1007/bf00219334
Abstract
No abstract availableKeywords
This publication has 30 references indexed in Scilit:
- Peroxisomal disorders: Complementation analysis using beta-oxidation of very long chain fatty acidsBiochemical and Biophysical Research Communications, 1990
- Zellweger-like syndrome with detectable hepatic peroxisomes: A variant form of peroxisomal disorderThe Journal of Pediatrics, 1988
- Genetic heterogeneity in the cerebrohepatorenal (Zellweger) syndrome and other inherited disorders with a generalized impairment of peroxisomal functions. A study using complementation analysis.Journal of Clinical Investigation, 1988
- Kinetics of the assembly of peroxisomes after fusion of complementary cell lines from patients with the cerebro-hepato-renal (Zellweger) syndrome and related disordersBiochemical and Biophysical Research Communications, 1988
- Biochemical abnormalities in rhizomelic chondrodysplasia punctataThe Journal of Pediatrics, 1988
- Peroxisomal β-oxidation enzyme proteins in the Zellweger syndromeBiochemical and Biophysical Research Communications, 1985
- Deficiency of Enzymes Catalyzing the Biosynthesis of Glycerol-Ether Lipids in Zellweger SyndromeNew England Journal of Medicine, 1984
- Infantile phytanic acid storage disease, a possible variant of Refsum's disease: Three cases, including ultrastructural studies of the liverJournal of Inherited Metabolic Disease, 1982
- Peroxisomal and Mitochondrial Defects in the Cerebro-Hepato-Renal SyndromeScience, 1973
- Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4Nature, 1970