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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Bibliographische Detailangaben
Hauptverfasser: Schmidt, Axel (VerfasserIn) , Hempel, Maja (VerfasserIn) , Tibelius, Alexandra (VerfasserIn) , Schwaibold, Eva (VerfasserIn) , Schaaf, Christian P. (VerfasserIn) , Zawada, Michal (VerfasserIn) , Kaufmann, Lilian (VerfasserIn) , Hinderhofer, Katrin (VerfasserIn) , Okun, Pamela M. (VerfasserIn) , Kotzaeridou, Urania (VerfasserIn) , Hoffmann, Georg F. (VerfasserIn) , Choukair, Daniela (VerfasserIn) , Bettendorf, Markus (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 24 June 2025
In: Nature genetics
Year: 2025, Jahrgang: 57, Heft: 7, Pages: 1790-1791
ISSN:1546-1718
DOI:10.1038/s41588-025-02271-6
Online-Zugang:Verlag, kostenfrei, Volltext: https://doi.org/10.1038/s41588-025-02271-6
Verlag, kostenfrei, Volltext: https://www.nature.com/articles/s41588-025-02271-6
Volltext
Verfasserangaben: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]

MARC

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