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Correspondence on “Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment” by Roux et al.
| Autores principales: | , , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Nature Publishing Group US
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8187144/ https://www.ncbi.nlm.nih.gov/pubmed/33564152 http://dx.doi.org/10.1038/s41436-021-01104-1 |
| _version_ | 1783705083380236288 |
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| author | Park, Joohyun Deininger, Natalie Rautenberg, Maren Saft, Carsten Harmuth, Florian Sturm, Marc Riess, Olaf Schöls, Ludger Synofzik, Matthis Haack, Tobias B. |
| author_facet | Park, Joohyun Deininger, Natalie Rautenberg, Maren Saft, Carsten Harmuth, Florian Sturm, Marc Riess, Olaf Schöls, Ludger Synofzik, Matthis Haack, Tobias B. |
| author_sort | Park, Joohyun |
| collection | PubMed |
| description | |
| format | Online Article Text |
| id | pubmed-8187144 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2021 |
| publisher | Nature Publishing Group US |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-81871442021-06-25 Correspondence on “Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment” by Roux et al. Park, Joohyun Deininger, Natalie Rautenberg, Maren Saft, Carsten Harmuth, Florian Sturm, Marc Riess, Olaf Schöls, Ludger Synofzik, Matthis Haack, Tobias B. Genet Med Correspondence Nature Publishing Group US 2021-02-09 2021 /pmc/articles/PMC8187144/ /pubmed/33564152 http://dx.doi.org/10.1038/s41436-021-01104-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
| spellingShingle | Correspondence Park, Joohyun Deininger, Natalie Rautenberg, Maren Saft, Carsten Harmuth, Florian Sturm, Marc Riess, Olaf Schöls, Ludger Synofzik, Matthis Haack, Tobias B. Correspondence on “Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment” by Roux et al. |
| title | Correspondence on “Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment” by Roux et al. |
| title_full | Correspondence on “Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment” by Roux et al. |
| title_fullStr | Correspondence on “Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment” by Roux et al. |
| title_full_unstemmed | Correspondence on “Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment” by Roux et al. |
| title_short | Correspondence on “Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment” by Roux et al. |
| title_sort | correspondence on “clinical, neuropathological, and genetic characterization of stub1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment” by roux et al. |
| topic | Correspondence |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8187144/ https://www.ncbi.nlm.nih.gov/pubmed/33564152 http://dx.doi.org/10.1038/s41436-021-01104-1 |
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