POST-MORTEM RECOGNITION OF INHERITED METABOLIC DISORDERS FROM SPECIFIC ACYLCARNITINES IN TISSUE IN CASES OF SUDDEN INFANT DEATH
- 1 February 1987
- journal article
- Published by Elsevier in The Lancet
- Vol. 329 (8531) , 512
- https://doi.org/10.1016/s0140-6736(87)92126-x
Abstract
No abstract availableKeywords
This publication has 3 references indexed in Scilit:
- Recognition of medium-chain acyl-CoA dehydrogenase deficiency in asymptomatic siblings of children dying of sudden infant death or Reye-like syndromesThe Journal of Pediatrics, 1986
- Defects of metabolism of fatty acids in the sudden infant death syndrome.BMJ, 1985
- Diagnostic and Therapeutic Implications of Medium-Chain Acylcarnitines in the Medium-Chain Acyl-CoA Dehydrogenase DeficiencyPediatric Research, 1985