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作者更正:RFC1基因内含子重复序列的双等位基因扩增是迟发性共济失调的常见病因。

Author Correction: Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxia.

作者信息

Cortese Andrea, Simone Roberto, Sullivan Roisin, Vandrovcova Jana, Tariq Huma, Yau Wai Yan, Humphrey Jack, Jaunmuktane Zane, Sivakumar Prasanth, Polke James, Ilyas Muhammad, Tribollet Eloise, Tomaselli Pedro J, Devigili Grazia, Callegari Ilaria, Versino Maurizio, Salpietro Vincenzo, Efthymiou Stephanie, Kaski Diego, Wood Nick W, Andrade Nadja S, Buglo Elena, Rebelo Adriana, Rossor Alexander M, Bronstein Adolfo, Fratta Pietro, Marques Wilson J, Züchner Stephan, Reilly Mary M, Houlden Henry

机构信息

Department of Neuromuscular Disease, UCL Queen Square Institute of Neurology and The National Hospital for Neurology and Neurosurgery, London, UK.

Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology and The National Hospital for Neurology and Neurosurgery, London, UK.

出版信息

Nat Genet. 2019 May;51(5):920. doi: 10.1038/s41588-019-0422-y.

DOI:10.1038/s41588-019-0422-y
PMID:31028356
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6730635/
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.

摘要

在本文最初发表的版本中,作者Wai Yan Yau的名字拼写错误。该错误已在文章的HTML和PDF版本中更正。

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