Substrate reduction therapy of glycosphingolipid storage disorders
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/s10545-006-0272-5
Reference78 articles.
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2. Abe A, Wild S, Lee W, Shayman J (2001) Agents for the treatment of glycosphingolipid storage disorders. Curr Drug Metab 2: 331–338.
3. Aerts JMFG, Hollak CEM (1997) Plasma and metabolic abnormalities in Gaucher's disease. Baillières Clin Haematol 10: 691–709.
4. Aerts JM, van Weely S, Boot R, Hollak CE, Tager JM (1993) Pathogenesis of lysosomal storage disorders as illustrated by Gaucher disease. J Inherit Met Dis 16: 288–291.
5. Aguilera B, Ghauharali-van der Vlugt K, Helmond MT, et al (2003) Transglycosidase activity of chitotriosidase: improved enzymatic assay for the human macrophage chitinase. J Biol Chem 278: 40911–40916.
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