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Erschienen in: Orphanet Journal of Rare Diseases 1/2024

Open Access 01.12.2024 | Correction

Correction: The impact of osteogenesis imperfecta severity on oral health-related quality of life in Spain: a cross-sectional study

verfasst von: Amira Ahmed Elfituri, Manuel Joaquín De Nova, Mohammadamin Najirad

Erschienen in: Orphanet Journal of Rare Diseases | Ausgabe 1/2024

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The original article can be found online at https://​doi.​org/​10.​1186/​s13023-024-03096-y.
Correction: Orphanet J Rare Dis 19, 108 (2024)
https://doi.org/10.1186/s13023-024-03096-y
Following publication of the original article [1], we have been notified that Table 3 was missing data in the row “Filled teeth”.
It should be as follows:
Filled teeth 7,80 11,40 16,33* 0,05
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://​creativecommons.​org/​licenses/​by/​4.​0/​. The Creative Commons Public Domain Dedication waiver (http://​creativecommons.​org/​publicdomain/​zero/​1.​0/​) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
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Titel
Correction: The impact of osteogenesis imperfecta severity on oral health-related quality of life in Spain: a cross-sectional study
verfasst von
Amira Ahmed Elfituri
Manuel Joaquín De Nova
Mohammadamin Najirad
Publikationsdatum
01.12.2024
Verlag
BioMed Central
Erschienen in
Orphanet Journal of Rare Diseases / Ausgabe 1/2024
Elektronische ISSN: 1750-1172
DOI
https://doi.org/10.1186/s13023-024-03186-x

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