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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.

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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
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  2. Laura Vilarinho
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Corresponding author

Correspondence to Manuela Schubert Baldo.

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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

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

Orphanet Journal of Rare Diseases

ISSN: 1750-1172