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Author correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings

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Main Authors: Schmidt, Axel (Author) , Hempel, Maja (Author) , Tibelius, Alexandra (Author) , Schwaibold, Eva (Author) , Schaaf, Christian P. (Author) , Zawada, Michal (Author) , Kaufmann, Lilian (Author) , Hinderhofer, Katrin (Author) , Okun, Pamela M. (Author) , Kotzaeridou, Urania (Author) , Hoffmann, Georg F. (Author) , Choukair, Daniela (Author) , Bettendorf, Markus (Author)
Format: Article (Journal)
Language:English
Published: 24 June 2025
In: Nature genetics
Year: 2025, Volume: 57, Issue: 7, Pages: 1790-1791
ISSN:1546-1718
DOI:10.1038/s41588-025-02271-6
Online Access:Verlag, kostenfrei, Volltext: https://doi.org/10.1038/s41588-025-02271-6
Verlag, kostenfrei, Volltext: https://www.nature.com/articles/s41588-025-02271-6
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Author Notes:Axel Schmidt, Maja Hempel, Alexandra Tibelius, Eva M.C. Schwaibold, Christian P. Schaaf, Michal Zawada, Lilian Kaufmann, Katrin Hinderhofer, Pamela M. Okun, Urania Kotzaeridou, Georg F. Hoffmann, Daniela Choukair, Markus Bettendorf [und sehr viele weitere Personen]
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Item Description:Veröffentlicht: 24. Juni 2025
Gesehen am 11.11.2025
Physical Description:Online Resource
ISSN:1546-1718
DOI:10.1038/s41588-025-02271-6

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