Correction to: 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)

Robert J. Pignolo; Geneviève Baujat; Matthew A. Brown; Carmen De Cunto; Maja Di Rocco; Edward C. Hsiao; Richard Keen; Mona Al Mukaddam; Kim Hanh Le Quan Sang; Amy Wilson; Barbara White; Donna R. Grogan; Frederick S. Kaplan

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Correction to: 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)

Orphanet Journal of Rare Diseases

DOI: 10.1186/s13023-019-1096-3

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Abstract

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.

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Pignolo, R. J., Baujat, G., Brown, M. A., De Cunto, C., Di Rocco, M., Hsiao, E. C., … Kaplan, F. S. (2019, May 23). Correction to: 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). Orphanet Journal of Rare Diseases. BioMed Central Ltd. https://doi.org/10.1186/s13023-019-1096-3

Correction to: 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)

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