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Correction to: Natural history of fibrodysplasia ossificans progressiva: cross-sectional analysis of annotated baseline phenotypes

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The original article was published in Orphanet Journal of Rare Diseases 2019 14:98

Corretion to: Orphanet J Rare Dis (2019) 14:98

https://doi.org/10.1186/s13023-019-1068-7

The original version of this article [1] unfortunately included an error to an author’s name. Author Maja Di Rocco was erroneously presented as Maja DiRocco.

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

For additional clarity, the Correction article also provides below an updated Table 2.

Table 2 Demographics and Baseline Disease by Age Category

Reference

  1. 1.

    Pignolo RJ, et al. Natural history of fibrodysplasia ossificans progressiva: cross-sectional analysis of annotated baseline phenotypes. Orphanet J Rare Dis. 2019;14:98. https://doi.org/10.1186/s13023-019-1068-7.

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Author information

Correspondence to Robert J. Pignolo or Frederick S. Kaplan.

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Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.

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Pignolo, R.J., Baujat, G., Brown, M.A. et al. Correction to: Natural history of fibrodysplasia ossificans progressiva: cross-sectional analysis of annotated baseline phenotypes. Orphanet J Rare Dis 14, 113 (2019) doi:10.1186/s13023-019-1096-3

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