Correction: Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment

The Original Article was published on 27 July 2020

Correction to: Genetics in Medicine 22, 1851–1862 (2020); https://doi.org/10.1038/s41436-020-0899-x; published online 27 July 2020

The original version of this Article contained an error in the author name for Lionel Van Maldergem. The family name was incorrectly spelled Van Maldergen. This has now been corrected in both the PDF and HTML versions of the Article.

Author information

Affiliations

Authors

Consortia

Corresponding author

Correspondence to Alexandra Durr MD, PhD.

Rights and permissions

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Roux, T., Barbier, M., Papin, M. et al. Correction: Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment. Genet Med (2020). https://doi.org/10.1038/s41436-020-01064-y

Download citation

Further reading

  • Expanding the clinical spectrum of STIP1 homology and U-box containing protein 1-associated ataxia

    • Jean-Marie Ravel
    • , Mehdi Benkirane
    • , Nadège Calmels
    • , Cecilia Marelli
    • , Fabienne Ory-Magne
    • , Claire Ewenczyk
    • , Yosra Halleb
    • , François Tison
    • , Claire Lecocq
    • , Guillaume Pische
    • , Philippe Casenave
    • , Annabelle Chaussenot
    • , Solène Frismand
    • , Louise Tyvaert
    • , Lise Larrieu
    • , Morgane Pointaux
    • , Nathalie Drouot
    • , Carine Bossenmeyer-Pourié
    • , Abderrahim Oussalah
    • , Jean-Louis Guéant
    • , Bruno Leheup
    • , Céline Bonnet
    • , Mathieu Anheim
    • , Christine Tranchant
    • , Laëtitia Lambert
    • , Jamel Chelly
    • , Michel Koenig
    •  & Mathilde Renaud

    Journal of Neurology (2021)

Search

Quick links