Article
Genetic relationship between the Zellweger syndrome and other peroxisomal disorders characterized by an impairment in the assembly of peroxisomes.
Progress in clinical and biological research - 1 Jan 1990
Tager J M, Brul S, Wiemer E A, Strijland A, Van Driel R, Schutgens R B, Van den Bosch H, Wanders R J, Westerveld A
Abstract excerpt
The peroxisomal diseases can be divided into three categories: 1) diseases in which morphologically distinguishable peroxisomes are virtually absent (Zellweger syndrome; infantile Refsum disease; Hyperpipecolic Acidaemia; neonatal Adrenoleukodystrophy); 2) diseases in which peroxisomes are presen...
Topics
- Alleles
- Cell Line
- Fibroblasts
- Fluorescent Antibody Technique
- Genetic Complementation Test
- Humans
- Metabolism, Inborn Errors
- Microbodies
- Phenotype
- Zellweger Syndrome