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

Orphanet Journal of Rare Diseases volume 14, Article number: 113 (2019) Cite this article

The Original Article was published on 03 May 2019

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.

For additional clarity, the Correction article also provides below an updated Table 2.

Table 2 Demographics and Baseline Disease by Age Category
Full size table

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. https://doi.org/10.1186/s13023-019-1068-7.

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Authors and Affiliations

  1. Department of Medicine, Mayo Clinic, Rochester, MN, USA

    Robert J. Pignolo

  2. Departement de Genetique, Institut IMAGINE and Hôpital Necker-Enfants Malades, Paris, France

    Geneviève Baujat & Kim-Hanh Le Quan Sang

  3. Institute of Health and Biomedical Innovation (IHBI), Translational Research Institute, Princess Alexandra Hospital, Queensland University of Technology (QUT), Queensland, Australia

    Matthew A. Brown

  4. Pediatric Rheumatology Section, Department of Pediatrics, Hospital Italiano de Buenos Aires, Buenos Aires, Argentina

    Carmen De Cunto

  5. Unit of Rare Diseases, Department of Pediatrics, Giannina Gaslini Institute, Genoa, Italy

    Maja Di Rocco

  6. Division of Endocrinology and Metabolism, the UCSF Metabolic Bone Clinic, The Institute of Human Genetics, and the UCSF Program in Craniofacial Biology, Department of Medicine, University of California-San Francisco, San Francisco, California, USA

    Edward C. Hsiao

  7. Centre for Metabolic Bone Disease, Royal National Orthopaedic Hospital, Stanmore, UK

    Richard Keen

  8. Departments of Medicine and Orthopaedic Surgery, The Center for Research in FOP and Related Disorders, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA

    Mona Al Mukaddam

  9. Clementia Pharmaceuticals Inc, Newton, MA, USA

    Amy Wilson, Barbara White & Donna R. Grogan

  10. Departments of Orthopaedic Surgery & Medicine, The Center for Research in FOP and Related Disorders, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA

    Frederick S. Kaplan

Authors
  1. Robert J. Pignolo
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  2. Geneviève Baujat
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  3. Matthew A. Brown
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  4. Carmen De Cunto
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  5. Maja Di Rocco
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  6. Edward C. Hsiao
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  7. Richard Keen
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  8. Mona Al Mukaddam
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  9. Kim-Hanh Le Quan Sang
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  10. Amy Wilson
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  11. Barbara White
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  12. Donna R. Grogan
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  13. Frederick S. Kaplan
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Corresponding authors

Correspondence to Robert J. Pignolo or Frederick S. Kaplan.

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Pignolo, R.J., Baujat, G., Brown, M.A. et al. Correction to: Natural history of fibrodysplasia ossificans progressiva: cross-sectional analysis of annotated baseline phenotypes. Orphanet J Rare Dis 14, 113 (2019). https://doi.org/10.1186/s13023-019-1096-3

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  • DOI: https://doi.org/10.1186/s13023-019-1096-3

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