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Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/38354
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dc.contributor.authorLewis, Barry Denison.en
dc.date.issued1997en
dc.identifier.urihttp://hdl.handle.net/2440/38354-
dc.descriptionAddendum pasted inside the back end-paper.en
dc.descriptionx, 179 leavesen
dc.description.abstractThis thesis presents a hypothesis that there are abnormalities of N-glycosylation in classical galactosaemia and that these abnormalities could contribute to the long-term complications. The aim of the thesis is to characterise and model N-glycosylation in skin fibroblasts from patients with galactosaemia. The study identifies a disturbance in the synthesis and processing of dolichol-linked oligosaccharides. It is anticipated that the serum glycoproteins in untreated galactosaemia may contain N-glycans that are partly absent or truncated.en
dc.format.extent471380 bytesen
dc.format.mimetypeapplication/pdfen
dc.language.isoenen
dc.subject.lcshGalactosemia Complications.en
dc.subject.lcshGlycosylation.en
dc.subject.lcshFibroblasts.en
dc.subject.lcshOligosaccharides.en
dc.subject.lcshGlycoproteins.en
dc.titleGlycoprocessing in classical galactosaemia / Barry Denison Lewisen
dc.typeThesisen
dc.contributor.schoolDept. of Paediatricsen
dc.provenanceThis electronic version is made publicly available by the University of Adelaide in accordance with its open access policy for student theses. Copyright in this thesis remains with the author. This thesis may incorporate third party material which has been used by the author pursuant to Fair Dealing exception. If you are the author of this thesis and do not wish it to be made publicly available or If you are the owner of any included third party copyright material you wish to be removed from this electronic version, please complete the take down form located at: http://www.adelaide.edu.au/legals-
dc.description.dissertationThesis (M.D.) -- University of Adelaide, Dept. of Paediatrics, 1997en
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