Intermediates of unsaturated fatty acid oxidation are incorporated in triglycerides but not in phospholipids in tissues from patients with mitochondrial β-oxidation defects-Reference-Cited by-同舟云学术

Intermediates of unsaturated fatty acid oxidation are incorporated in triglycerides but not in phospholipids in tissues from patients with mitochondrial β-oxidation defects

Published:2001-06 Issue:3 Volume:24 Page:337-344
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J Inherit Metab Dis

Author:

Onkenhout W.¹,Venizelos V.¹,Scholte H. R.²,de Klerk J. B. C.³,Poorthuis B. J. H. M.¹

Affiliation:

1. ; Department of Pediatrics, P3-P; Leiden University Medical Center; Leiden

2. ; Department of Biochemistry; Erasmus University Rotterdam; The Netherlands

3. ; Department of Pediatrics; Erasmus University Rotterdam; The Netherlands

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1023/A:1010592232317/fullpdf

Reference19 articles.

1. Clear correlation of genotype with disease phenotype in very-long-chain acyl-CoA dehydrogenase deficiency;Andresen;Am J Hum Genet,1999

2. Biochemical diagnosis of fatty acid oxidation disorders by metabolite analysis of postmortem liver;Boles;Hum Pathol,1994

3. Retrospective biochemical screening of fatty acid oxidation disorders in postmortem livers of 418 cases of sudden death in the first year of life;Boles;J Pediatr,1998

4. Biosynthesis of the unsaturated 14-carbon fatty acids found on the N termini of photoreceptor-specific proteins;DeMar;J Biol Chem,1996

5. Determination of total fatty acids in plasma: cis-5-tetradecenoic acid (C14:1ω-9) in the diagnosis of long-chain fatty acid oxidation defects;Divry;J Inherit Metab. Dis,1999

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