Genetic relationship between the Zellweger syndrome and other peroxisomal disorders characterized by an impairment in the assembly of peroxisomes.

Abstract

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 present but several peroxisomal functions are impaired (rhizomelic… (More)

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Cite this paper

@article{Tager1990GeneticRB, title={Genetic relationship between the Zellweger syndrome and other peroxisomal disorders characterized by an impairment in the assembly of peroxisomes.}, author={Joseph M. Tager and Stanley Brul and Erik A C Wiemer and Anneke Strijland and Roel van Driel and Ruud B. H. Schutgens and Han van den Bosch and Ronald J. A. Wanders and Andries Westerveld}, journal={Progress in clinical and biological research}, year={1990}, volume={321}, pages={545-58} }