Mutations in medium chain acyl-CoA dehydrogenase deficiency
Open Access
- 1 September 1990
- journal article
- letter
- Published by Elsevier in The Lancet
- Vol. 336 (8717) , 748-749
- https://doi.org/10.1016/0140-6736(90)92241-9
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- Molecular lesion in patients with medium-chain acyl-CoA dehydrogenase deficiencyThe Lancet, 1990
- Application of fast atom bombardment with tandem mass spectrometry and liquid chromatography/ mass spectrometry to the analysis of acylcarnitines in human urine, blood, and tissueAnalytical Biochemistry, 1989
- Medium-Chain Acyl-CoA Dehydrogenase DeficiencyNew England Journal of Medicine, 1988
- A new patient with dicarboxylic aciduria suggestive of medium-chain acyl-CoA dehydrogenase deficiency presenting as Reye's syndromeJournal of Inherited Metabolic Disease, 1984