Title : Immunological cell type characterization and Th1-Th17 cytokine production in a mouse model of Gaucher disease.

Pub. Date : 2012 Jul

PMID : 22595426






1 Functional Relationships(s)
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1 Gaucher disease is a lysosomal storage disease resulting from insufficient acid beta-glucosidase (glucocerebrosidase, GCase, EC 4.2.1.25) activity and the resultant accumulation of glucosylceramide. Glucosylceramides glucosidase, beta, acid Mus musculus