Gaucher Disease
Author:
Publisher
Wiley
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/9781119697312.ch9
Reference35 articles.
1. Immunological Cells and Functions in Gaucher Disease
2. Replacement Therapy for Inherited Enzyme Deficiency — Macrophage-Targeted Glucocerebrosidase for Gaucher's Disease
3. Novel oral treatment of Gaucher's disease with N-butyldeoxynojirimycin (OGT 918) to decrease substrate biosynthesis
4. Gaucher disease: single gene molecular characterization of one-hundred Indian patients reveals novel variants and the most prevalent mutation
5. ER retention and degradation as the molecular basis underlying Gaucher disease heterogeneity
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1. Glycosphingolipids within membrane contact sites influence their function as signaling hubs in neurodegenerative diseases;FEBS Open Bio;2023-04-17
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