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Original Article

Peroxisomal dysfunction in chondrodysplasia punctata, rhizomelic type

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Pages 183-185 | Accepted 11 Nov 1986, Published online: 08 Jul 2009

References

  • Heymans H. S. A., Oorthuys J. W. E., Nelck G., Wanders R. J. A., Schutgens R. B. H. Rhizomelic chondrodysplasia punctata: another peroxisomal disorder. New. Engl. J. Med. 1985; 313: 187–188
  • Moser H. W. Peroxisomal disorders. J. Pediat. 1986; 108: 89–91
  • Schutgens R. B. H., Heymans H. S. A., Wanders R. J. A., Van Den Bosch H., Tager J. M. Peroxisomal disorders: a newly recognized group of genetic diseases. Eur. J. Pediat. 1986; 144: 430–440
  • Wanders R. J. A., Saelman D., Heymans H. S. A., Schutgens R. B. H., Westerveld A., Poll-The B. T., Saudubray J. M., Van Den Bosch H., Strijland A., Schram A. W., Tager J. M. Genetic relation between the Zellweger syndrome, infantile Refsum disease and rhizomelic chondrodysplasia punctata. New Engl. J. Med. 1986; 314: 78

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