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Glycobiology: Enzyme deficiencies deciphered
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Medical Biochemistry and Microbiology.
2012 (English)In: Nature chemical biology, ISSN 1552-4469, Vol. 8, no 2, 137-138 p.Article in journal (Refereed) Published
Abstract [en]

Mucopolysaccharidoses are inherited disorders in which inactivation of lysosomal enzymes results in accumulation of glycosaminoglycans within cells, causing tissue and organ dysfunction. A method to determine the unique end structures of the accumulated glycosaminoglycans offers a new way for diagnosis.

Place, publisher, year, edition, pages
2012. Vol. 8, no 2, 137-138 p.
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Medical and Health Sciences
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URN: urn:nbn:se:uu:diva-194279DOI: 10.1038/nchembio.778PubMedID: 22257851OAI: oai:DiVA.org:uu-194279DiVA: diva2:604788
Available from: 2013-02-12 Created: 2013-02-12 Last updated: 2013-02-13Bibliographically approved

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Kjellén, Lena

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