Isolated Isobutyryl-CoA Dehydrogenase Deficiency: An Unrecognized Defect in Human Valine Metabolism-Reference-Cited by-同舟云学术

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Isolated Isobutyryl-CoA Dehydrogenase Deficiency: An Unrecognized Defect in Human Valine Metabolism

Published:1998-12 Issue:4 Volume:65 Page:264-271
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Roe Charles R.,Cederbaum Stephen D.,Roe Diane S.,Mardach Rebecca,Galindo Alvaro,Sweetman Lawrence

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference12 articles.

1. Isovaleric acidemia: A new genetic defect of leucine metabolism;Tanaka;Proc Natl Acad Sci USA,1966

2. Jamaican vomiting sickness: Biochemical investigation of two cases;Tanaka;New Engl J Med,1976

3. Glutaric aciduria type II: Report on a previously undescribed metabolic disorder;Przyrembel;Clin Chim Acta,1976

4. Nuclear encoded defects of the mitochondrial respiratory chain, including glutaric acidemia type II;Frerman,1995

5. Separation and properties of five distinct acyl-CoA dehydrogenases from rat liver mitochondria. Identification of a new 2-methyl branched chain acyl-CoA dehydrogenase;Ikeda;J Biol Chem,1983

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