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Case Reports

. 1990;13(3):311-4.

doi: 10.1007/BF01799383.

Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: identification of a new inborn error of mitochondrial fatty acid beta-oxidation

R J Wanders¹, L IJlst, A H van Gennip, C Jakobs, J P de Jager, L Dorland, F J van Sprang, M Duran

Affiliations

PMID: 2122092
DOI: 10.1007/BF01799383

Case Reports

Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: identification of a new inborn error of mitochondrial fatty acid beta-oxidation

R J Wanders et al. J Inherit Metab Dis. 1990.

. 1990;13(3):311-4.

doi: 10.1007/BF01799383.

Authors

R J Wanders¹, L IJlst, A H van Gennip, C Jakobs, J P de Jager, L Dorland, F J van Sprang, M Duran

Affiliation

¹ Department of Paediatrics, University Hospital Amsterdam, The Netherlands.

PMID: 2122092
DOI: 10.1007/BF01799383

No abstract available

PubMed Disclaimer

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References

1. Biochim Biophys Acta. 1982 Nov 12;713(2):270-9 - PubMed
1. Arch Biochem Biophys. 1980 Aug;203(1):372-83 - PubMed
1. J Inherit Metab Dis. 1990;13(1):4-36 - PubMed
1. Eur J Biochem. 1980 Feb;103(3):589-96 - PubMed
1. J Inherit Metab Dis. 1987;10 Suppl 1:159-200 - PubMed

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