Oxidation of unsaturated fatty acids by human fibroblasts with very-long-chain acyl-CoA dehydrogenase deficiency: aspects of substrate specificity and correlation with clinical phenotype-Reference-Cited by-同舟云学术

Oxidation of unsaturated fatty acids by human fibroblasts with very-long-chain acyl-CoA dehydrogenase deficiency: aspects of substrate specificity and correlation with clinical phenotype

Published:2001-10 Issue:1-2 Volume:312 Page:55-67
ISSN:0009-8981
Container-title:Clinica Chimica Acta
language:en
Short-container-title:Clinica Chimica Acta

Author:

Roe Diane S,Vianey-Saban Christine,Sharma Shailja,Zabot Marie-Therese,Roe Charles R

Publisher

Elsevier BV

Subject

Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine

Reference26 articles.

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3. Genomic DNA organization of human mitochondrial very-long-chain acyl-CoA dehydrogenase and mutation analysis;Orii;Biochem. Biophys. Res. Commun.,1995

4. Assignment of the human mitochondrial very-long-chain acyl-CoA dehydrogenase gene (LCACD) to 17p13 by in situ hybridization;Aoyama;Genomics,1996

5. Long-chain acyl-coenzyme A dehydrogenase deficiency: an inherited cause of nonketotic hypoglycemia;Hale;Pediatr. Res.,1985

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