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dc.date.accessioned2013-03-12T12:14:39Z
dc.date.available2013-03-12T12:14:39Z
dc.date.issued2012en_US
dc.date.submitted2012-03-09en_US
dc.identifier.citationKoht, Jeanette. Hereditary ataxias, epidemiological and genetic studies in a Norwegian population. Doktoravhandling, University of Oslo, 2012en_US
dc.identifier.urihttp://hdl.handle.net/10852/28034
dc.language.isoengen_US
dc.relation.haspartPaper 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.haspartPaper 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.haspartPaper 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.haspartPaper 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.urihttps://doi.org/10.1093/brain/awp056
dc.relation.urihttps://doi.org/10.1111/j.1600-0404.2009.01214.x
dc.relation.urihttps://doi.org/10.1111/j.1600-0404.2011.01504.x
dc.titleHereditary ataxias, epidemiological and genetic studies in a Norwegian populationen_US
dc.typeDoctoral thesisen_US
dc.date.updated2012-06-21en_US
dc.creator.authorKoht, Jeanetteen_US
dc.subject.nsiVDP::700en_US
cristin.unitcode130000en_US
cristin.unitnameMedisinske fakulteten_US
dc.identifier.bibliographiccitationinfo: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=Doktoravhandlingen_US
dc.identifier.urnURN:NBN:no-30928en_US
dc.type.documentDoktoravhandlingen_US
dc.identifier.duo152616en_US
dc.contributor.supervisorChantal Tallaksen, Giovanni Stevanin, Alexandra Durr, Alexis Briceen_US
dc.identifier.bibsys121771229en_US
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/28034/1/dravhandling-koht.pdf


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