Immunoelectron-microscopic detection of globotriaosylceramide accumulated in the skin of patients with Fabry disease
Author:
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2133.2005.06732.x/fullpdf
Reference13 articles.
1. Enzymatic defect in Fabry's disease. Ceramidetrihexosidase deficiency;Brady;N Engl J Med,1967
2. Fabry's disease: classification as a sphingolipidosis and partial characterization of a novel glycolipid;Sweeley;J Biol Chem,1963
3. Fabry disease: ultrastructural lectin histochemical analyses of lysosomal deposits;Kanda;Virchows Arch,2000
4. Generation of one set of murine monoclonal antibodies specific for globo-series glycolipids: evidence for differential distribution of the glycolipids in rat small intestine;Kotani;Arch Biochem Biophys,1994
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Multiple phenotypic domains of Fabry disease and their relevance for establishing genotype–phenotype correlations
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