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Correction to: An ontological foundation for ocular phenotypes and rare eye diseases

Orphanet Journal of Rare Diseases volume 14, Article number: 200 (2019) Cite this article

The Original Article was published on 09 January 2019

Correction to: Orphanet J Rare Dis

https://doi.org/10.1186/s13023-018-0980-6

Professor Michael Larsen, who is a member of the ERN-EYE Ontology Study Group and co-chair of Workgroup on Retinal Rare Eye Diseases (WG1), was inadvertently omitted from the author list in the Acknowledgements section of the original article [1].

Reference

  1. Sergouniotis, et al. An ontological foundation for ocular phenotypes and rare eye diseases. Orphanet J Rare Dis. 2019;14:8 https://doi.org/10.1186/s13023-018-0980-6.

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Authors and Affiliations

  1. University of Manchester and Manchester Royal Eye Hospital, Oxford Road, Manchester, M13 9WL, UK

    Panagiotis I. Sergouniotis

  2. Orphanet, INSERM (Institut National de la Santé et de la Recherche Médicale), Paris, France

    Emmanuel Maxime, Annie Olry & Ana Rath

  3. Centre for Rare Eye Diseases CARGO, SENSGENE FSMR Network, Strasbourg University Hospital, Strasbourg, France

    Dorothée Leroux & Hélène Dollfus

  4. Newcastle University, Newcastle upon Tyne, UK

    Rachel Thompson

  5. The Jackson Laboratory for Genomic Medicine, Farmington, CT, USA

    Peter N. Robinson

  6. Laboratoire de Génétique Médicale, Faculté de Médecine de Strasbourg, INSERM U1112, 11 rue Humann, 67 085, Strasbourg, France

    Hélène Dollfus

Authors
  1. Panagiotis I. Sergouniotis
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  2. Emmanuel Maxime
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  3. Dorothée Leroux
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  4. Annie Olry
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  5. Rachel Thompson
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  6. Ana Rath
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  7. Peter N. Robinson
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  8. Hélène Dollfus
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for the ERN-EYE Ontology Study Group

Corresponding authors

Correspondence to Panagiotis I. Sergouniotis or Hélène Dollfus.

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Sergouniotis, P.I., Maxime, E., Leroux, D. et al. Correction to: An ontological foundation for ocular phenotypes and rare eye diseases. Orphanet J Rare Dis 14, 200 (2019). https://doi.org/10.1186/s13023-019-1156-8

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  • DOI: https://doi.org/10.1186/s13023-019-1156-8

Orphanet Journal of Rare Diseases

ISSN: 1750-1172