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

Research output: Contribution to journalComment/debatepeer-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 languageEnglish (US)
Article number113
JournalOrphanet Journal of Rare Diseases
Volume14
Issue number1
DOIs
StatePublished - May 23 2019

ASJC Scopus subject areas

  • Genetics(clinical)
  • Pharmacology (medical)

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