Peroxisomal matrix enzymes in Zellweger syndrome: activity and subcellular localization in liver.

Journal of inherited metabolic disease ·Vol. 8 Suppl 2 ·1985-00-00 ·Pages 151-2

Wanders RJ, Schutgens RB, Tager JM

Abstract

暂无摘要

MeSH Terms

Acyltransferases/deficiency Alcohol Oxidoreductases/analysis Catalase/analysis D-Amino-Acid Oxidase/analysis Facial Bones/abnormalities Hepatomegaly Humans Kidney Diseases, Cystic/enzymology Liver/enzymology Liver Diseases/congenital Microbodies/enzymology Skull/abnormalities Syndrome

Chemicals

Alcohol Oxidoreductases L-2-hydroxyacid oxidase Catalase D-Amino-Acid Oxidase Acyltransferases glycerone-phosphate O-acyltransferase

Authors & Affiliations

3 authors, click to expand affiliations / ORCID

Wanders R J

Schutgens R B

Tager J M

References (3)

3 references, click to expand

Activity of peroxisomal enzymes and intracellular distribution of catalase in Zellweger syndrome.
Biochem Biophys Res Commun. 1984 Sep 28;123(3):1054-61 PMID: 6148939
Review: the cerebrohepatorenal syndrome of Zellweger, morphologic and metabolic aspects.
Am J Med Genet. 1983 Dec;16(4):503-17 PMID: 6362411
Deficiency of acyl-CoA: dihydroxyacetone phosphate acyltransferase in patients with Zellweger (cerebro-hepato-renal) syndrome.
Biochem Biophys Res Commun. 1984 Apr 16;120(1):179-84 PMID: 6712687

Article Info

Journal

Journal of inherited metabolic disease

Abbr.

J Inherit Metab Dis

ISSN

0141-8955

DOI

10.1007/BF01811504

Published

1985-00-00

Pages

151-2

Language

English

Region

United States

NLM ID

7910918

Subset

External Links

PubMed source DOI: 10.1007/BF01811504 View journal details

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Peroxisomal matrix enzymes in Zellweger syndrome: activity and subcellular localization in liver.

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