dc.contributor.author | Paucar, Martin | |
dc.contributor.author | Tesi, Bianca | |
dc.contributor.author | Eshtad, Saeed | |
dc.contributor.author | Eriksson, Caroline | |
dc.contributor.author | Hashim, Farouk | |
dc.contributor.author | Nilsson, Daniel | |
dc.contributor.author | Pourhamidi, Kaveh | |
dc.contributor.author | Hellström-Lindberg, Eva | |
dc.contributor.author | Bryceson, Yenan | |
dc.contributor.author | Svenningsson, Per | |
dc.date.accessioned | 2022-04-19T13:17:01Z | |
dc.date.available | 2022-04-19T13:17:01Z | |
dc.date.created | 2022-02-07T14:06:57Z | |
dc.date.issued | 2021 | |
dc.identifier.issn | 2376-7839 | |
dc.identifier.uri | https://hdl.handle.net/11250/2991361 | |
dc.description.abstract | Variants in tumor suppressor genes and in genes encoding DNA repairing proteins are associated with syndromes conferring neurologic features and increased risk for malignancy. The best example for these conditions is ataxia-telangiectasia (AT). A more rare and recent disease is an ataxia-pancytopenia syndrome (ATXPC) associated with heterozygous gain-of-function variants in the tumor suppressor gene SAMD9L (MIM 159550). Here, we describe a patient with a complex cerebellar syndrome associated with a novel SAMD9L pathogenic variant. | en_US |
dc.language.iso | eng | en_US |
dc.publisher | Wolters Kluwer | en_US |
dc.rights | Attribution-NonCommercial-NoDerivatives 4.0 Internasjonal | * |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/deed.no | * |
dc.title | Adult-Onset Ataxia with Neuropathy and White Matter Abnormalities Due to a Novel SAMD9L Variant | en_US |
dc.type | Journal article | en_US |
dc.type | Peer reviewed | en_US |
dc.description.version | publishedVersion | en_US |
dc.rights.holder | Copyright 2021 The Author(s) | en_US |
dc.source.articlenumber | e628 | en_US |
cristin.ispublished | true | |
cristin.fulltext | original | |
cristin.qualitycode | 1 | |
dc.identifier.doi | 10.1212/NXG.0000000000000628 | |
dc.identifier.cristin | 1998611 | |
dc.source.journal | Neurology: Genetics | en_US |
dc.identifier.citation | Neurology: Genetics. 2021, 7 (6), e628. | en_US |
dc.source.volume | 7 | en_US |
dc.source.issue | 6 | en_US |