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Correction to:An ontological foundation for ocular phenotypes and rare eye diseases (Orphanet Journal of Rare Diseases (2019) 14 (8) DOI: 10.1186/s13023-018-0980-6)
- Source :
- Sergouniotis, P I, Maxime, E, Leroux, D, Olry, A, Thompson, R, Rath, A, Robinson, P N & Dollfus, H 2019, ' Correction to : An ontological foundation for ocular phenotypes and rare eye diseases (Orphanet Journal of Rare Diseases (2019) 14 (8) DOI: 10.1186/s13023-018-0980-6) ', Orphanet Journal of Rare Diseases, vol. 14, no. 1, 200 . https://doi.org/10.1186/s13023-019-1156-8
- Publication Year :
- 2019
-
Abstract
- 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].
- Subjects :
- Genetics(clinical)
Pharmacology (medical)
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Journal :
- Sergouniotis, P I, Maxime, E, Leroux, D, Olry, A, Thompson, R, Rath, A, Robinson, P N & Dollfus, H 2019, ' Correction to : An ontological foundation for ocular phenotypes and rare eye diseases (Orphanet Journal of Rare Diseases (2019) 14 (8) DOI: 10.1186/s13023-018-0980-6) ', Orphanet Journal of Rare Diseases, vol. 14, no. 1, 200 . https://doi.org/10.1186/s13023-019-1156-8
- Accession number :
- edsair.od......3818..2883f640387547597541465e823fa059
- Full Text :
- https://doi.org/10.1186/s13023-018-0980-6)