Biochemical studies on cultured skin fibroblasts from a baby with long-chain acyl-CoA dehydrogenase deficiency presenting as sudden neonatal death
- 1 June 1987
- journal article
- Published by Springer Nature in Journal of Inherited Metabolic Disease
- Vol. 10 (S2), 260-262
- https://doi.org/10.1007/bf01811420
Abstract
No abstract availableThis publication has 3 references indexed in Scilit:
- Long-Chain Acyl Coenzyme A Dehydrogenase Deficiency: An Inherited Cause of Nonketotic HypoglycemiaPediatric Research, 1985
- Defects of metabolism of fatty acids in the sudden infant death syndrome.BMJ, 1985
- Fluorometric assay of acyl-CoA dehydrogenases in normal and mutant human fibroblastsBiochemical Medicine, 1985