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

doi: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)

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

Hospital Internal Medicine

Research output: Contribution to journal › Comment/debate › peer-review

2 Scopus citations

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.

Original language	English (US)
Article number	113
Journal	Orphanet Journal of Rare Diseases
Volume	14
Issue number	1
DOIs	https://doi.org/10.1186/s13023-019-1096-3
State	Published - May 23 2019

ASJC Scopus subject areas

Genetics(clinical)
Pharmacology (medical)

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Pignolo, R. J., Baujat, G., Brown, M. A., De Cunto, C., Di Rocco, M., Hsiao, E. C., Keen, R., Al Mukaddam, M., Sang, K. H. L. Q., Wilson, A., White, B., Grogan, D. R., & Kaplan, F. S. (2019). 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, 14(1), Article 113. 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). / Pignolo, Robert J.; Baujat, Geneviève; Brown, Matthew A. et al.
In: Orphanet Journal of Rare Diseases, Vol. 14, No. 1, 113, 23.05.2019.

Research output: Contribution to journal › Comment/debate › peer-review

Pignolo, RJ, Baujat, G, Brown, MA, De Cunto, C, Di Rocco, M, Hsiao, EC, Keen, R, Al Mukaddam, M, Sang, KHLQ, Wilson, A, White, B, Grogan, DR & Kaplan, FS 2019, '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, vol. 14, no. 1, 113. https://doi.org/10.1186/s13023-019-1096-3

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title = "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)",

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.",

author = "Pignolo, {Robert J.} and Genevi{\`e}ve Baujat and Brown, {Matthew A.} and {De Cunto}, Carmen and {Di Rocco}, Maja and Hsiao, {Edward C.} and Richard Keen and {Al Mukaddam}, Mona and Sang, {Kim Hanh Le Quan} and Amy Wilson and Barbara White and Grogan, {Donna R.} and Kaplan, {Frederick S.}",

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AU - Pignolo, Robert J.

AU - Baujat, Geneviève

AU - Brown, Matthew A.

AU - De Cunto, Carmen

AU - Di Rocco, Maja

AU - Hsiao, Edward C.

AU - Keen, Richard

AU - Al Mukaddam, Mona

AU - Sang, Kim Hanh Le Quan

AU - Wilson, Amy

AU - White, Barbara

AU - Grogan, Donna R.

AU - Kaplan, Frederick S.

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AB - 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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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)

Abstract

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