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 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

Research output: Contribution to journalComment/debate

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 languageEnglish (US)
Article number113
JournalOrphanet Journal of Rare Diseases
Volume14
Issue number1
DOIs
StatePublished - May 23 2019

Fingerprint

Myositis Ossificans
Names
Cross-Sectional Studies
Phenotype

ASJC Scopus subject areas

  • Genetics(clinical)
  • Pharmacology (medical)

Cite this

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

In: Orphanet Journal of Rare Diseases, Vol. 14, No. 1, 113, 23.05.2019.

Research output: Contribution to journalComment/debate

Pignolo, Robert ; Baujat, Geneviève ; Brown, Matthew A. ; De Cunto, Carmen ; Di Rocco, Maja ; Hsiao, Edward C. ; Keen, Richard ; Al Mukaddam, Mona ; Sang, Kim Hanh Le Quan ; Wilson, Amy ; White, Barbara ; Grogan, Donna R. ; Kaplan, Frederick S. / 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). In: Orphanet Journal of Rare Diseases. 2019 ; Vol. 14, No. 1.
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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 = "Robert Pignolo 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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T2 - 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)

AU - Pignolo, Robert

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.

PY - 2019/5/23

Y1 - 2019/5/23

N2 - 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.

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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