Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/32945
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dc.contributor.authorHopwood, J.-
dc.date.issued2001-
dc.identifier.citationJournal of Inherited Metabolic Disease, 2001; 24(SUPPL. 2):45-46-
dc.identifier.issn0141-8955-
dc.identifier.issn1573-2665-
dc.identifier.urihttp://hdl.handle.net/2440/32945-
dc.language.isoen-
dc.publisherKluwer Academic Publ-
dc.rights© 2001 SSIEM and Kluwer Academic Publishers-
dc.source.urihttp://dx.doi.org/10.1023/a:1012459521922-
dc.titleSelection of endpoints in clinical studies of enzyme replacement therapy in lysosomal storage disorders - Commentary-
dc.typeJournal article-
dc.identifier.doi10.1023/A:1012459521922-
pubs.publication-statusPublished-
Appears in Collections:Aurora harvest 6
Paediatrics publications

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