Molecular basis of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: identification of the major disease-causing mutation in the α-subunit of the mitochondrial trifunctional protein
- 17 December 1994
- journal article
- research article
- Published by Elsevier in Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism
- Vol. 1215 (3) , 347-350
- https://doi.org/10.1016/0005-2760(94)90064-7
Abstract
No abstract availableKeywords
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