Glycogen Storage Disease Type II
- Name
- Glycogen Storage Disease Type II
- Accession Number
- DBCAT001324
- Description
Not Available
- Drugs
Drug Drug Description Alglucosidase alfa An acid alpha- glucosidase (GAA) derivative used as an enzyme replacement therapy for the treatment of Pompe disease in infants and pediatric patients caused by GAA deficiency. - Drugs & Drug Targets
Drug Target Type Alglucosidase alfa Cation-dependent mannose-6-phosphate receptor target Alglucosidase alfa Glycogen target