Pages that link to "Q52095593"
Jump to navigation
Jump to search
The following pages link to Biochemical studies in a patient with subacute neuropathic Gaucher disease without visceral glucosylceramide storage. (Q52095593):
Displaying 4 items.
- Glucosylceramide transfer from lysosomes--the missing link in molecular pathology of glucosylceramidase deficiency: a hypothesis based on existing data (Q31072456) (← links)
- Genetic heterogeneity in type 1 Gaucher disease: multiple genotypes in Ashkenazic and non-Ashkenazic individuals (Q33564845) (← links)
- Posttranslational processing of human lysosomal acid beta-glucosidase: a continuum of defects in Gaucher disease type 1 and type 2 fibroblasts (Q35248348) (← links)
- Dependence of reversibility and progression of mouse neuronopathic Gaucher disease on acid beta-glucosidase residual activity levels (Q36961324) (← links)