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Orphanet Journal of Rare Diseases logoLink to Orphanet Journal of Rare Diseases
. 2019 May 23;14:113. doi: 10.1186/s13023-019-1096-3

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

Robert J Pignolo 1,, Geneviève Baujat 2, Matthew A Brown 3, Carmen De Cunto 4, Maja Di Rocco 5, Edward C Hsiao 6, Richard Keen 7, Mona Al Mukaddam 8, Kim-Hanh Le Quan Sang 2, Amy Wilson 9, Barbara White 9, Donna R Grogan 9, Frederick S Kaplan 10,
PMCID: PMC6532205  PMID: 31122250

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.

Contributor Information

Robert J. Pignolo, Email: pignolo.robert@mayo.edu

Frederick S. Kaplan, Email: frederick.kaplan@uphs.upenn.edu

Reference

  • 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. doi: 10.1186/s13023-019-1068-7. [DOI] [PMC free article] [PubMed] [Google Scholar]

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