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Table 7Second-level literature screen results

Study TypeFabry DiseaseType 1 Gaucher DiseaseType II Glycogen Storage Disease (Pompe)MPS IMPS IIMPS VITotal
RCT/Prospective phase I/II87854335
Case Series2953201071120
Case Reports161413128669
Guidelines43111111
Registry Reports34003111
Reviews41322218127132
Total10111364463519378

From: Findings

Cover of Enzyme-Replacement Therapies for Lysosomal Storage Diseases
Enzyme-Replacement Therapies for Lysosomal Storage Diseases [Internet].
Technical Briefs, No. 12.
Ratko TA, Marbella A, Godfrey S, et al.

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