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Outcome of type III Gaucher disease on enzyme replacement therapy: review of 55 cases.
Umeå University, Faculty of Medicine, Clinical Sciences, Paediatrics.
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2007 (English)In: J Inherit Metab Dis, ISSN 1573-2665, Vol. 30, no 6, 935-42 p.Article in journal (Other academic) Published
Place, publisher, year, edition, pages
2007. Vol. 30, no 6, 935-42 p.
Keyword [en]
Adolescent, Adult, Child, Child; Preschool, Enzymes/*therapeutic use, Female, Gaucher Disease/*drug therapy/*genetics, Glucosylceramidase/genetics, Heterozygote, Homozygote, Humans, Intelligence Tests, Male, Nervous System Diseases/pathology, Risk Factors, Time Factors, Treatment Outcome
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URN: urn:nbn:se:umu:diva-8963PubMedID: 17994286OAI: oai:DiVA.org:umu-8963DiVA: diva2:148634
Available from: 2008-02-22 Created: 2008-02-22 Last updated: 2011-01-11Bibliographically approved

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CiteExportLink to record
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