1980•Biochimica et Biophysica Acta (BBA) - Lipids and Lipid MetabolismRequires access

A lysosomal storage disorder in mice characterized by a dual deficiency of sphingomyelinase and glucocerebrosidase

Peter G. Pentchev, Andrew E. Gal, A. D. Booth, Fausta Omodeo‐Salè, J. Fours, B. Neumeyer, Jane M. Quirk, Glyn Dawson, Brady Ro

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Key concepts: Sphingomyelin, Glucocerebroside, Lactosylceramide, Glucocerebrosidase, Niemann–Pick disease, Sphingomyelin phosphodiesterase, Ganglioside, Ceramide

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A lysosomal storage disorder in mice characterized by a dual deficiency of sphingomyelinase and glucocerebrosidase — Research Paper | ScholarLens