Skip to main content
Download PDF

Correction to: Molecular basis of Leigh syndrome: a current look

Orphanet Journal of Rare Diseases volume 15, Article number: 77 (2020) Cite this article

The Original Article was published on 29 January 2020

Correction to: Orphanet J Rare Dis (2020) 15:31

https://doi.org/10.1186/s13023-020-1297-9

The original version of this article [1] unfortunately included an error to an author’s name. Author Manuela Schubert Baldo was erroneously presented as Manuela Baldo Schubert.

The author name has been updated in the original article and included in the author list of this Correction article.

Reference

  1. Schubert, Vilarinho. Molecular basis of Leigh syndrome: a current look. Orphanet J Rare Dis. 2020;15:31 https://doi.org/10.1186/s13023-020-1297-9.

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

  1. Newborn screening, metabolism and genetics unit - human genetics department, Instituto Nacional de Saúde Doutor Ricardo Jorge (INSA), Porto, Portugal

    Manuela Schubert Baldo & Laura Vilarinho

Authors
  1. Manuela Schubert Baldo
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Laura Vilarinho
    View author publications

    You can also search for this author in PubMed Google Scholar

Corresponding author

Correspondence to Manuela Schubert Baldo.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and Permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Schubert Baldo, M., Vilarinho, L. Correction to: Molecular basis of Leigh syndrome: a current look. Orphanet J Rare Dis 15, 77 (2020). https://doi.org/10.1186/s13023-020-1351-7

Download citation

  • Published:

  • DOI: https://doi.org/10.1186/s13023-020-1351-7

Orphanet Journal of Rare Diseases

ISSN: 1750-1172