Secondary sphingolipid accumulation in a macrophage model of Gaucher disease
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism
Reference34 articles.
1. Metabolism of glucocerebrosides. II. Evidence of an enzymatic deficiency in Gaucher’s disease;Brady;Biochem. Biophys. Res. Commun.,1965
2. Short communications: a deficiency of glucocerebrosidase in Gaucher’s disease;Patrick;Biochem. J.,1965
3. Gaucher disease;Beutler,2001
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5. Gaucher’s disease in an asymptomatic 72-year-old;Beutler;JAMA,1977
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