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

doi:10.1038/s41588-019-0422-y

Published Erratum

. 2019 May;51(5):920.

doi: 10.1038/s41588-019-0422-y.

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

Andrea Cortese¹, Roberto Simone², Roisin Sullivan³, Jana Vandrovcova³, Huma Tariq³, Wai Yan Yau³, Jack Humphrey³, Zane Jaunmuktane², Prasanth Sivakumar³, James Polke⁴, Muhammad Ilyas⁵, Eloise Tribollet³, Pedro J Tomaselli⁶, Grazia Devigili⁷, Ilaria Callegari⁸, Maurizio Versino^{8

9}, Vincenzo Salpietro³, Stephanie Efthymiou³, Diego Kaski³, Nick W Wood³, Nadja S Andrade¹⁰, Elena Buglo¹¹, Adriana Rebelo¹¹, Alexander M Rossor³, Adolfo Bronstein², Pietro Fratta³, Wilson J Marques⁶, Stephan Züchner¹¹, Mary M Reilly³, Henry Houlden^{12

13}

Affiliations

¹ Department of Neuromuscular Disease, UCL Queen Square Institute of Neurology and The National Hospital for Neurology and Neurosurgery, London, UK. andrea.cortese@ucl.ac.uk.
² Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology and The National Hospital for Neurology and Neurosurgery, London, UK.
³ Department of Neuromuscular Disease, UCL Queen Square Institute of Neurology and The National Hospital for Neurology and Neurosurgery, London, UK.
⁴ Neurogenetics Laboratory, UCL Queen Square Institute of Neurology and The National Hospital for Neurology and Neurosurgery, London, UK.
⁵ Department of Biological Sciences, International Islamic University, Islamabad, Pakistan.
⁶ Department of Neurology, School of Medicine at Ribeirão Preto, University of São Paulo, Ribeirão Preto, Brazil.
⁷ UO Neurologia I, Fondazione IRCCS Istituto Neurologico 'Carlo Besta', Milan, Italy.
⁸ IRCCS Mondino Foundation, Pavia, Italy.
⁹ Department of Brain and Behavioral Sciences, University of Pavia, Pavia, Italy.
¹⁰ Department of Psychiatry and Behavioural Sciences, Center for Therapeutic Innovation, University of Miami Miller School of Medicine, Miami, FL, USA.
¹¹ Dr. John T. Macdonald Foundation Department of Human Genetics and John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, FL, USA.
¹² Department of Neuromuscular Disease, UCL Queen Square Institute of Neurology and The National Hospital for Neurology and Neurosurgery, London, UK. h.houlden@ucl.ac.uk.
¹³ Neurogenetics Laboratory, UCL Queen Square Institute of Neurology and The National Hospital for Neurology and Neurosurgery, London, UK. h.houlden@ucl.ac.uk.

PMID: 31028356
PMCID: PMC6730635
DOI: 10.1038/s41588-019-0422-y

Published Erratum

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

Andrea Cortese et al. Nat Genet. 2019 May.

. 2019 May;51(5):920.

doi: 10.1038/s41588-019-0422-y.

Authors

Affiliations

¹ Department of Neuromuscular Disease, UCL Queen Square Institute of Neurology and The National Hospital for Neurology and Neurosurgery, London, UK. andrea.cortese@ucl.ac.uk.
² Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology and The National Hospital for Neurology and Neurosurgery, London, UK.
³ Department of Neuromuscular Disease, UCL Queen Square Institute of Neurology and The National Hospital for Neurology and Neurosurgery, London, UK.
⁴ Neurogenetics Laboratory, UCL Queen Square Institute of Neurology and The National Hospital for Neurology and Neurosurgery, London, UK.
⁵ Department of Biological Sciences, International Islamic University, Islamabad, Pakistan.
⁶ Department of Neurology, School of Medicine at Ribeirão Preto, University of São Paulo, Ribeirão Preto, Brazil.
⁷ UO Neurologia I, Fondazione IRCCS Istituto Neurologico 'Carlo Besta', Milan, Italy.
⁸ IRCCS Mondino Foundation, Pavia, Italy.
⁹ Department of Brain and Behavioral Sciences, University of Pavia, Pavia, Italy.
¹⁰ Department of Psychiatry and Behavioural Sciences, Center for Therapeutic Innovation, University of Miami Miller School of Medicine, Miami, FL, USA.
¹¹ Dr. John T. Macdonald Foundation Department of Human Genetics and John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, FL, USA.
¹² Department of Neuromuscular Disease, UCL Queen Square Institute of Neurology and The National Hospital for Neurology and Neurosurgery, London, UK. h.houlden@ucl.ac.uk.
¹³ Neurogenetics Laboratory, UCL Queen Square Institute of Neurology and The National Hospital for Neurology and Neurosurgery, London, UK. h.houlden@ucl.ac.uk.

PMID: 31028356
PMCID: PMC6730635
DOI: 10.1038/s41588-019-0422-y

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.

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Erratum for

Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxia.
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, Züchner S, Reilly MM, Houlden H. Cortese A, et al. Nat Genet. 2019 Apr;51(4):649-658. doi: 10.1038/s41588-019-0372-4. Epub 2019 Mar 29. Nat Genet. 2019. PMID: 30926972 Free PMC article.

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Intronic pentanucleotide expansion in the replication factor 1 gene (RFC1) is a major cause of adult-onset ataxia.
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Author Correction: Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxia

Affiliations

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

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