Mitochondrial very-long-chain acyl-coenzyme A dehydrogenase deficiency: clinical characteristics and diagnostic considerations in 30 patients-Reference-Cited by-同舟云学术

Mitochondrial very-long-chain acyl-coenzyme A dehydrogenase deficiency: clinical characteristics and diagnostic considerations in 30 patients

Published:1998-01 Issue:1 Volume:269 Page:43-62
ISSN:0009-8981
Container-title:Clinica Chimica Acta
language:en
Short-container-title:Clinica Chimica Acta

Author:

Vianey-Saban Christine,Divry Priscille,Brivet Michèle,Nada Mohamed,Zabot Marie-Thérèse,Mathieu Monique,Roe Charles

Publisher

Elsevier BV

Subject

Biochemistry, medical,Clinical Biochemistry,Biochemistry,General Medicine

Reference41 articles.

1. The inborn errors of mitochondrial fatty acid oxidation;Vianey-Liaud;J Inher Metab Dis,1987

2. Roe CR, Coates PM. Mitochondrial fatty acid oxidation disorders. In: Scriver CR, Beaudet AL, Sly WS, Valle D editors. The metabolic and molecular bases of inherited disease. New York: McGraw-Hill, 1995:1501–1533.

3. Beta oxidation of fatty acids;Schultz;Biochim Biophys Acta,1991

4. Novel fatty acid β-oxidation enzymes in rat liver mitochondria. I. Purification and properties of very-long-chain acyl-coenzyme A dehydrogenase;Izai;J Biol Chem,1992

5. Novel fatty acid β-oxidation enzymes in rat liver mitochondria. II. Purification and properties of enoyl-Coenzyme A (CoA) hydratase/3-hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase trifunctional protein;Uchida;J Biol Chem,1992

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