Defective Peroxisome Membrane Synthesis Due To Mutations in Human PEX3 Causes Zellweger Syndrome, Complementation Group G
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics
Reference26 articles.
1. Ultrastructural and cytochemical demonstration of peroxisomes in cultured fibroblasts from patients with peroxisomal deficiency disorders;Arias;J Cell Biol,1985
2. The Hansenula polymorpha PER9 gene encodes a peroxisomal membrane protein essential for peroxisome assembly and integrity;Baerends;J Biol Chem,1996
3. A novel beta thalassemia gene with a single base mutation in the conserved polypyrimidine sequence at the 3′ end of IVS 2;Beldjord;Nucleic Acids Res,1988
4. Human adrenoleukodystrophy protein and related peroxisomal ABC transporters interact with the peroxisomal assembly protein PEX19p;Glöckner;Biochem Biophys Res Commun,2000
5. Pex19p, a farnesylated protein essential for peroxisome biogenesis;Götte;Mol Cell Biol,1998
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