J. D. Jager

SUDDEN INFANT DEATH AND LONG-CHAIN 3-HYDROXYACYL-CoA DEHYDROGENASE

R. Wanders, M. Durán, L. Ijlst, 1989, The Lancet.

3-Hydroxydicarboxylic aciduria due to long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency associated with sudden neonatal death: protective effect of medium-chain triglyceride treatment

R. Wanders, M. Durán, D. Ketting, 2005, European Journal of Pediatrics.

dehydrogenase deficiency Retinal dystrophy in long chain 3-hydroxy-acyl-coA

J. Smeitink, G. V. Lith, J. D. Jager, 2006 .

Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: Identification of a new inborn error of mitochondrial fatty acidβ-oxidation

R. Wanders, L. Ijlst, C. Jakobs, 1990, Journal of Inherited Metabolic Disease.