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Original Article

Fractionation of 4-methylumbelliferyl-ß-galactosidase Activities in Liver in Gargoylism

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Pages 199-202 | Received 24 Jul 1968, Accepted 31 Aug 1968, Published online: 05 Aug 2009

References

  • öckerman P. A. β-galactosidase and α-manno-sidase deficiency-primary enzyme defects in gar-goylism and a new storage disease. Acta paediat. (Uppsala) 1967, Suppl 177: 35–36
  • Öckerman P. A. Acid hydrolases in skin and plasma in gargoylism. Deficiency of β-galacto-sidase in skin. Clin. chim. Acta 1968; 20: 1–6
  • Öckerman P. A. Identity of β-glucosidase, β-xylosidase and one of the β-galactosidase activities in human liver when assayed with 4-methylumbelli-feryl-β-D-glycosides. Studies in cases of Gaucher's disease. Biochim. biophys. Acta (Amst.) 1968; 165: 59–62
  • Öckerman P. A. Lysosomal acid hydrolases in the liver in gargoylism. Deficiency of 4–methyl-umbelliferyl-β-galactosidase. Scand. J. clin. Lab. In vest. 1968; 22: 142
  • Robinson D., Price R. G., Dance N. Separation and properties of β-galactosidase, β-gluco-sidase, β-glucuronidase and N-acetyl-β-glucosami-nidase from rat kidney. Biochem. J. 1967; 102: 525–532
  • Vanhoof F., Hers H. G. Lysosomal enzymes in gargoylism. 4th Meeting Feder. Europ. Biochem. Soc., Oslo, July, 3–71967

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