Accumulation of 3-Hydroxy-Fatty Acids in the Culture Medium of Long-Chain l-3-Hydroxyacyl CoA Dehydrogenase (LCHAD) and Mitochondrial Trifunctional Protein-Deficient Skin Fibroblasts: Implications for Medium Chain Triglyceride Dietary Treatment of LCHAD Deficiency-Reference-Cited by-同舟云学术

Accumulation of 3-Hydroxy-Fatty Acids in the Culture Medium of Long-Chain l-3-Hydroxyacyl CoA Dehydrogenase (LCHAD) and Mitochondrial Trifunctional Protein-Deficient Skin Fibroblasts: Implications for Medium Chain Triglyceride Dietary Treatment of LCHAD Deficiency

Published:2003-05 Issue:5 Volume:53 Page:783-787
ISSN:0031-3998
Container-title:Pediatric Research
language:
Short-container-title:Pediatr Res

Author:

Jones Patricia M,Butt Yasmeen,Bennett Michael J

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology, and Child Health

Reference17 articles.

1. Fatty Acid Oxidation Disorders

2. Inborn Errors of Mitochondrial Fatty Acid Oxidation

3. Genetic disorders of mitochondrial fatty acid oxidation

4. Fatty acid oxidation disorders: A new class of metabolic diseases

5. Recognition and management of fatty acid oxidation defects: A series of 107 patients

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