Familial hypoketotic hypoglycaemia associated with peripheral neuropathy, pigmentary retinopathy and C6–C14 hydroxydicarboxylic aciduria. A new defect in fatty acid oxidation?
- 1 June 1988
- journal article
- research article
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 11 (S2), 183-185
- https://doi.org/10.1007/bf01804230
Abstract
No abstract availableKeywords
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- Peroxisomal disorders: A newly recognised group of genetic diseasesEuropean Journal of Pediatrics, 1986
- The acyl-CoA dehydrogenation deficiencies. Recent advances in the enzymic characterization and understanding of the metabolic and pathophysiological disturbances in patients with acyl-CoA dehydrogenation deficiencies.1985
- Formation of cholic acid from 3 alpha, 7 alpha, 12 alpha-trihydroxy-5 beta-cholestanoic acid by rat liver peroxisomes.Journal of Lipid Research, 1983