dc.date.accessioned | 2013-03-12T12:14:39Z | |
dc.date.available | 2013-03-12T12:14:39Z | |
dc.date.issued | 2012 | en_US |
dc.date.submitted | 2012-03-09 | en_US |
dc.identifier.citation | Koht, Jeanette. Hereditary ataxias, epidemiological and genetic studies in a Norwegian population. Doktoravhandling, University of Oslo, 2012 | en_US |
dc.identifier.uri | http://hdl.handle.net/10852/28034 | |
dc.language.iso | eng | en_US |
dc.relation.haspart | Paper I Erichsen AK, Koht J, Stray-Pedersen A, Abdelnoor M, Tallaksen CM. Prevalence of hereditary ataxia and spastic paraplegia in southeast Norway: a population-based study Brain. 2009 Jun;132(Pt 6):1577-88. The paper is removed from the thesis in DUO due to publisher restrictions. The published version is available at: https://doi.org/10.1093/brain/awp056 | |
dc.relation.haspart | Paper II Koht J, Bjørnarå KA, Jørum E, Tallaksen CM. Ataxia with vitamin E deficiency in southeast Norway, case report Acta Neurol Scand Suppl. 2009;(189):42-5. The paper is removed from the thesis in DUO due to publisher restrictions. The published version is available at: https://doi.org/10.1111/j.1600-0404.2009.01214.x | |
dc.relation.haspart | Paper III Koht J, Stevanin G, Durr A, Mundwiller E, Brice A, Tallaksen CM. SCA14 in Norway, two families with autosomal dominant cerebellar ataxia and a novel mutation in the PRKCG gene Acta Neurol Scand. 2012 Feb;125(2):116-22. The paper is removed from the thesis in DUO due to publisher restrictions. The published version is available at: https://doi.org/10.1111/j.1600-0404.2011.01504.x | |
dc.relation.haspart | Paper IV Koht J, Tallaksen CM, Mundwiller E, Gaussen M, Tesson C, Brice A, Durr A, Stevanin G. A late onset autosomal dominant ataxia maps to chromosome 10q26.3. The paper is removed from the thesis in DUO due to publisher restrictions. | |
dc.relation.uri | https://doi.org/10.1093/brain/awp056 | |
dc.relation.uri | https://doi.org/10.1111/j.1600-0404.2009.01214.x | |
dc.relation.uri | https://doi.org/10.1111/j.1600-0404.2011.01504.x | |
dc.title | Hereditary ataxias, epidemiological and genetic studies in a Norwegian population | en_US |
dc.type | Doctoral thesis | en_US |
dc.date.updated | 2012-06-21 | en_US |
dc.creator.author | Koht, Jeanette | en_US |
dc.subject.nsi | VDP::700 | en_US |
cristin.unitcode | 130000 | en_US |
cristin.unitname | Medisinske fakultet | en_US |
dc.identifier.bibliographiccitation | info:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&rft.au=Koht, Jeanette&rft.title=Hereditary ataxias, epidemiological and genetic studies in a Norwegian population&rft.inst=University of Oslo&rft.date=2012&rft.degree=Doktoravhandling | en_US |
dc.identifier.urn | URN:NBN:no-30928 | en_US |
dc.type.document | Doktoravhandling | en_US |
dc.identifier.duo | 152616 | en_US |
dc.contributor.supervisor | Chantal Tallaksen, Giovanni Stevanin, Alexandra Durr, Alexis Brice | en_US |
dc.identifier.bibsys | 121771229 | en_US |
dc.identifier.fulltext | Fulltext https://www.duo.uio.no/bitstream/handle/10852/28034/1/dravhandling-koht.pdf | |