Diagnosis of medium chain acyl-CoA dehydrogenase deficiency in the newborn
- 26 May 1990
- journal article
- other
- Published by Elsevier in The Lancet
- Vol. 335 (8700) , 1288-1289
- https://doi.org/10.1016/0140-6736(90)91363-f
Abstract
No abstract availableKeywords
This publication has 3 references indexed in Scilit:
- The use of phenylpropionic acid as a loading test for medium-chain acyl-CoA dehydrogenase deficiencyJournal of Inherited Metabolic Disease, 1988
- The inborn errors of mitochondrial fatty acid oxidationJournal of Inherited Metabolic Disease, 1987
- SCREENING SIBLINGS FOR INBORN ERRORS OF FATTY ACID METABOLISM IN FAMILIES WITH A HISTORY OF SUDDEN INFANT DEATHThe Lancet, 1986