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Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxia (vol 51, pg 649, 2019)

Academic Article
Publication Date:
2019
abstract:
In the version of this article initially published, the name of author Wai Yan Yau was misspelled. The error has been corrected in the HTML and PDF versions of the article.
Iris type:
Articolo su Rivista
List of contributors:
Cortese, A; Simone, R; Sullivan, R; Vandrovcova, J; Tariq, H; Yau, Wy; Humphrey, J; Jaunmuktane, Z; Sivakumar, P; Polke, J; Ilyas, M; Tribollet, E; Tomaselli, Pj; Devigili, G; Callegari, I; Versino, M; Salpietro, V; Efthymiou, S; Kaski, D; Wood, Nw; Andrade, Ns; Buglo, E; Rebelo, A; Rossor, Am; Bronstein, A; Fratta, P; Marques, Wj; Zuchner, S; Reilly, Mm; Houlden, H
Authors of the University:
VERSINO MAURIZIO
Handle:
https://irinsubria.uninsubria.it/handle/11383/2103480
Published in:
NATURE GENETICS
Journal
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