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Barbier, Mathieu
Papin, Mélanie
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van Broeckhoven, Christine
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Duyckaerts, Charles
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Durr, Alexandra http://orcid.org/0000-0002-8921-7104
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Stevanin, Giovanni
Brice, Alexis
Darios, Frédéric
Forlani, Sylvie
Site, Pitié-Salpêtrière
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Marelli, Cecilia
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Rodriguez, Diana
Belarbi, Soraya
Hamri, Abdelmadjid
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Pandolfo, Massimo
Laura, Jardim
Guergueltcheva, Velina
Tournev, Ivalo
Pedraza Linarès, Olga Lucia
Nielsen, Jørgen E.
Svenstrup, Kirsten
Zaki, Maha
Bauer, Peter
Schöls, Lüdger
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Bertini, Enrico
Brusco, Alfredo
Casali, Carlo
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Criscuolo, Chiara
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Orsi, Laura
Santorelli, Filippo M.
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Coutinho, Paula
Loureiro, José Léal
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Rouco Axpe, Idoia
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Paucar, Martin Arce
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Bing-Wen, Soong
Reid, Evan
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Warner, Thomas
Wood, Nicholas
This article is maintained by: Elsevier
Article Title: Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment
Journal Title: Genetics in Medicine
CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/s41436-020-0899-x
Content Type: article
Copyright: © 2020, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics