Kolvraa S. Gregersen N, Christensen E, Hobolth N: Invitro fibroblast studies in a patient with C6-C10-dicarboxylic aciiduria: evidence for a defect in general acylCoA dehydrogenase. Clin Chim Acta 1982; 126: 53-62.
Howat AJ, Bennett MJ, Shaw L, Variend S: Mediumchain acylcoenzyme A deficiency presenting as sudden infant death syndrome (Letter). Br Med J 1984; 288: 397.
Wanders RJA, Duran M, Ijlst L, Jager JP, Gennip AH, Jakobs C. Dorland L, Sprang FJ: Sudden infant death and long-chain 3-hydroxyacyl-CoA dehydrogenase. Lancet1989;(i): 52-53.
Naylor EW, Chase DH: Automated tandem mass spectrometry fro mass newborn screening for disorders in fatty acid, organic acid, and aminoacid metabolism. J Child Neurol 1999; 14 (suppl): S4-S8.