REFERENCES
Amendt BA, Rhead WJ (1986) The multiple acyl-CoA dehydrogenation disorders, glutaric aciduria type II and ethylmalonic-adipic aciduria. J Clin Invest 78: 205–213.
Beckmann JD, Frerman FE (1985) Electron transfer flavoprotein ubiquinone oxidoreductase from pig liver: purification, molecular redox and catalytic properties. Biochemistry 24: 3913–3921.
Frerman FE, Goodman SI (1995) Nuclear encoded defects of the mitochondrial respiratory chain, including glutaric aciduria type II. In Scriver CR, Beaudet AL, Sly WS, Valle D, eds. The Metabolic and Molecular Bases of Inherited Disease, 7th edn. New York: McGraw-Hill, 1611–1629.
Lazarow PB, Moser HW (1995) Disorders of peroxisome biogenesis. In Scriver CR, Beaudet AL, Sly WS, Valle D, eds. The Metabolic and Molecular Bases of Inherited Disease, 7th edn. New York: McGraw-Hill, 2287–2324.
Paavola P (1997) Clinical and genetic herogeneity in Meckel syndrome. Hum Genet 101: 88–92.
Vianey-Saban C, Mousson B, Bertrand C, et al (1993) Carnitine palmitoyltransferase I deficiency presenting as a Reye-like syndrome without hypoglycemia. Eur J Pediatr 152: 334–338.
Witt DR, Theobald M, Santa Maria M, et al (1991) Carnitine palmitoyltransferase-type 2 deficiency: two new cases and successful prenatal diagnosis. Am J Hum Genet (Suppl) 49: 109.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Vianey-Saban, C., Bouvier, R., Cochat, P. et al. Antenatal expression of multiple acyl-CoA dehydrogenase deficiency. J Inherit Metab Dis 23, 345–348 (2000). https://doi.org/10.1023/A:1005623028638
Issue Date:
DOI: https://doi.org/10.1023/A:1005623028638