Mitochondrial morphology, bioenergetics and proteomic responses in fatty acid oxidation disorders
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,Clinical Biochemistry
Reference41 articles.
1. The biochemistry and physiology of mitochondrial fatty acid b-oxidation and its genetic disorders;Houten;Annu. Rev. Physiol.,2016
2. Carnitine transport and fatty acid oxidation;Longo;Biochim. Biophys. Acta,2016
3. Pathophysiology of fatty acid oxidation disorders;Bennett;J. Inherit. Metab. Dis.,2009
4. Molecular basis of human mitochondrial very-long-chain acyl-CoA dehydrogenase deficiency causing cardiomyopathy and sudden death in childhood;Strauss;Proc. Natl. Acad. Sci. U.S.A.,1995
5. The mutational spectrum in very-long-chain acyl-CoA dehydrogenase deficiency;Andresen;J. Inherit. Metab. Dis.,1996
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