Enzyme replacement therapy in Fabry disease: comparison of agalsidase alfa and agalsidase beta

Mol Genet Metab. 2008 Sep-Oct;95(1-2):114-5. doi: 10.1016/j.ymgme.2008.07.002. Epub 2008 Aug 12.
No abstract available

Publication types

  • Comparative Study
  • Letter
  • Comment

MeSH terms

  • Fabry Disease / drug therapy*
  • Humans
  • Isoenzymes / genetics
  • Isoenzymes / therapeutic use*
  • Recombinant Proteins
  • alpha-Galactosidase / genetics
  • alpha-Galactosidase / therapeutic use*

Substances

  • Isoenzymes
  • Recombinant Proteins
  • agalsidase alfa
  • alpha-Galactosidase
  • agalsidase beta