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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 in Orphanet Journal of Rare Diseases 2017 12:91

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. 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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Author information

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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Orphanet Journal of Rare Diseases

ISSN: 1750-1172