References
Goldbloom RB (1992) Unforgettable patients.J Pediatr 121: 827–828.
Lazarow PB, Moser MW (1989) Disorders of peroxisome biogenesis. In Scriver CR, Beaudet AL, Sly WS, Valle D, eds.The Metabolic Basis of Inherited Disease, 6th edn, McGraw-Hill, New York, 1479–1509.
Perheentupa J, Autio S, Leisti S, Raitta C, Tuuteri L (1973) Mulibrey nanism, an autosomal recessive syndrome with pericardial constriction.Lancet 2: 351–355.
Schrakamp G, Schalkwijk CG, Schutgens RBH, Wanders RJA, Tager JM, van den Bosch H (1988) Plasmalogen biosynthesis in peroxisomal disorders.J Lipid Res 29: 325–334.
Schutgens RBH, Wanders RJA, Nijenhuis AA et al (1987) Genetic diseases caused by peroxisomal dysfunction: new findings in clinical and biochemical studies.Enzyme 38: 161–176.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Schutgens, R.B.H., Ryynänen, M. & Wanders, R.J.A. Peroxisomal functions in Mulibrey nanism. J Inherit Metab Dis 17, 626 (1994). https://doi.org/10.1007/BF00711603
Issue Date:
DOI: https://doi.org/10.1007/BF00711603