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Erratum to: Quantification of gait in mitochondrial m.3243A > G patients: a validation study

Orphanet Journal of Rare Diseases volume 12, Article number: 170 (2017) Cite this article

The Original Article was published on 15 May 2017

Erratum

Upon publication of this article [1] it was noticed that Table 2 was incorrect. During Production, errors were introduced into the Variable column. The correct version of Table 2 can be seen below.

Table 2 Intra class correlations coefficients (ICCs) of the gait parameters for each walking condition
Full size table

Reference

  1. Ramakers R, Koene S, Groothuis J, et al. Quantification of gait in mitochondrial m.3243A > G patients: a validation study. Orphanet J Rare Dis. 2017;12:91.

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Authors and Affiliations

  1. Radboud Center for Mitochondrial Medicine (RCMM) at the Department of Pediatrics, Radboud University Medical Center Nijmegen, Geert Grooteplein Zuid 10, PO BOX 9101, 6500 HB, Nijmegen, The Netherlands

    Rob Ramakers, Saskia Koene, Jan T. Groothuis, Paul de Laat, Mirian C. H. Janssen & Jan Smeitink

  2. Radboud Center for Mitochondrial Medicine (RCMM) at the Department of Internal Medicine, Radboud University Medical Center Nijmegen, Geert Grooteplein Zuid 10, PO BOX 9101, 6500 HB, Nijmegen, The Netherlands

    Mirian C. H. Janssen

  3. Department of Rehabilitation, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, PO BOX 9101, 6500 HB, Nijmegen, The Netherlands

    Jan T. Groothuis

Authors
  1. Rob Ramakers
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  2. Saskia Koene
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  3. Jan T. Groothuis
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  4. Paul de Laat
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  5. Mirian C. H. Janssen
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  6. Jan Smeitink
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Corresponding author

Correspondence to Saskia Koene.

Additional information

The online version of the original article can be found under doi:10.1186/s13023-017-0644-y

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Ramakers, R., Koene, S., Groothuis, J.T. et al. Erratum to: Quantification of gait in mitochondrial m.3243A > G patients: a validation study. Orphanet J Rare Dis 12, 170 (2017). https://doi.org/10.1186/s13023-017-0688-z

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  • DOI: https://doi.org/10.1186/s13023-017-0688-z

Orphanet Journal of Rare Diseases

ISSN: 1750-1172