Answer
Idursulfase supplies the deficient enzyme iduronate-2-sulfatase, entering cellular lysosomes through mannose-6-phosphate receptor-mediated uptake to break down accumulated glycosaminoglycans in Hunter syndrome.
Sources for this answer
- Elaprase 2 mg/ml concentrate for solution for infusionTakeda UK Ltd · emc · SmPC §5.1 Pharmacodynamic properties · Version 21Document updated
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