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Analysis of a 43.6 kb deletion in a patient with Hunter syndrome (MPS II): the identification of a fusion transcript including sequences from the gene W and the IDS gene
Uppsala University, Medicinska vetenskapsområdet, Faculty of Medicine, Department of Genetics and Pathology. (Genetic disease)
Uppsala University, Medicinska vetenskapsområdet, Faculty of Medicine, Department of Genetics and Pathology. (Genetic disease)
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2000 (English)In: Hum Mutation, Vol. 15, 324- p.Article in journal (Refereed) Published
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2000. Vol. 15, 324- p.
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URN: urn:nbn:se:uu:diva-51472OAI: oai:DiVA.org:uu-51472DiVA: diva2:79381
Available from: 2008-10-17 Created: 2008-10-17 Last updated: 2011-01-14

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