Abstract
Sphingomyelinase hydrolyses sphingomyelin to ceramide and phosphoryl choline. In tissues from patients suffering from Niemann-Pick disease type A and B this lysosomal, membrane-associated enzyme is deficient and sphingomyelin accumulates1. In tissues from patients with Niemann-Pick disease type C, sphingomyelin also accumulates but sphingomyelinase is not deficient1.
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© 1986 Plenum Press, New York
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Al, E.J.M. et al. (1986). Immunological Studies on Lysosomal Sphingomyelinase: Immunization Procedures, Properties of Polyclonal and Monoclonal Antibodies Obtained and Effect of Triton X-100 on Binding of Enzyme Activity. In: Freysz, L., Dreyfus, H., Massarelli, R., Gatt, S. (eds) Enzymes of Lipid Metabolism II. NATO ASI Series, vol 116. Springer, Boston, MA. https://doi.org/10.1007/978-1-4684-5212-9_39
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DOI: https://doi.org/10.1007/978-1-4684-5212-9_39
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