The clinical spectrum of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency-Reference-Cited by-同舟云学术

The clinical spectrum of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency

Published:1996-04 Issue:3 Volume:14 Page:236-243
ISSN:0887-8994
Container-title:Pediatric Neurology
language:en
Short-container-title:Pediatric Neurology

Author:

Pons Roser,Roig Manuel,Riudor Encarnacio,Ribes Antonia,Briones Paz,Ortigosa Luis,Baldellou Antonio,Gil-Gibernau Juanjo,Olesti Mariona,Navarro Carmen,Wanders Ronald J.A.

Publisher

Elsevier BV

Subject

Neurology (clinical),Developmental Neuroscience,Neurology,Pediatrics, Perinatology and Child Health

Reference44 articles.

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4. Novel fatty acid betaoxidation enzymes in rat liver mitochondria. II. Purification and properties of enoyl CoA hydratase-3-hydroxyacyl-CoA dehydrogenase-3ketoacyl-CoA thiolase trifunctional protein;Uchida;J Biol Chem,1992

5. Disorders of fatty acid oxidation;Stanley,1990

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