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Biallelic POLR3A variants confirmed as a frequent cause of hereditary ataxia and spastic paraparesis
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6439323/ https://www.ncbi.nlm.nih.gov/pubmed/30847471 http://dx.doi.org/10.1093/brain/awz041 |
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author | Rydning, Siri L Koht, Jeanette Sheng, Ying Sowa, Piotr Hjorthaug, Hanne S Wedding, Iselin M Erichsen, Anne Kjersti Hovden, Inger Anette Backe, Paul H Tallaksen, Chantal M E Vigeland, Magnus D Selmer, Kaja K |
author_facet | Rydning, Siri L Koht, Jeanette Sheng, Ying Sowa, Piotr Hjorthaug, Hanne S Wedding, Iselin M Erichsen, Anne Kjersti Hovden, Inger Anette Backe, Paul H Tallaksen, Chantal M E Vigeland, Magnus D Selmer, Kaja K |
author_sort | Rydning, Siri L |
collection | PubMed |
description | |
format | Online Article Text |
id | pubmed-6439323 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-64393232019-04-04 Biallelic POLR3A variants confirmed as a frequent cause of hereditary ataxia and spastic paraparesis Rydning, Siri L Koht, Jeanette Sheng, Ying Sowa, Piotr Hjorthaug, Hanne S Wedding, Iselin M Erichsen, Anne Kjersti Hovden, Inger Anette Backe, Paul H Tallaksen, Chantal M E Vigeland, Magnus D Selmer, Kaja K Brain Letters to the Editor Oxford University Press 2019-04 2019-03-07 /pmc/articles/PMC6439323/ /pubmed/30847471 http://dx.doi.org/10.1093/brain/awz041 Text en © The Author(s) (2019). Published by Oxford University Press on behalf of the Guarantors of Brain. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Letters to the Editor Rydning, Siri L Koht, Jeanette Sheng, Ying Sowa, Piotr Hjorthaug, Hanne S Wedding, Iselin M Erichsen, Anne Kjersti Hovden, Inger Anette Backe, Paul H Tallaksen, Chantal M E Vigeland, Magnus D Selmer, Kaja K Biallelic POLR3A variants confirmed as a frequent cause of hereditary ataxia and spastic paraparesis |
title | Biallelic POLR3A variants confirmed as a frequent cause of hereditary ataxia and spastic paraparesis |
title_full | Biallelic POLR3A variants confirmed as a frequent cause of hereditary ataxia and spastic paraparesis |
title_fullStr | Biallelic POLR3A variants confirmed as a frequent cause of hereditary ataxia and spastic paraparesis |
title_full_unstemmed | Biallelic POLR3A variants confirmed as a frequent cause of hereditary ataxia and spastic paraparesis |
title_short | Biallelic POLR3A variants confirmed as a frequent cause of hereditary ataxia and spastic paraparesis |
title_sort | biallelic polr3a variants confirmed as a frequent cause of hereditary ataxia and spastic paraparesis |
topic | Letters to the Editor |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6439323/ https://www.ncbi.nlm.nih.gov/pubmed/30847471 http://dx.doi.org/10.1093/brain/awz041 |
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