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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
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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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