Deficiency of acyl-CoA: Dihydroxyacetone phosphate acyltransferase in patients with Zellweger (cerebro-hepato-renal) syndrome
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
Reference17 articles.
1. Peroxisomal and Mitochondrial Defects in the Cerebro-Hepato-Renal Syndrome
2. Cerebro-hepato-renal syndrome of Zellweger
3. A metabolic disorder similar to Zellweger syndrome with hepatic acatalasia and absence of peroxisomes, altered content and redox state of cytochromes, and infantile cirrhosis with hemosiderosis
4. Defects of Bile Acid Synthesis in Zellweger's Syndrome
5. Zur Morphologie und Diagnostik des Zellweger Syndroms
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