Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings
Axel Schmidt, Florian Kraft, Annekatrin Ripke, Ingo Kurth(Universität Hamburg), Sarina Schwartzmann(Charité - Universitätsmedizin Berlin), Henrike L. Sczakiel(Humboldt-Universität zu Berlin), Yorck Hellenbroich(University of Lübeck), Matthias Begemann(RWTH Aachen University), Daniela Choukair(Heidelberg University), Miriam Elbracht(RWTH Aachen University), Katharina Mayerhanser(Technical University of Munich), Martin A. Mensah(Humboldt-Universität zu Berlin), Pamela M. Okun, Julia Hoefele(Institute of Human Genetics), Malte Spielmann(Christian-Albrechts-Universität zu Kiel), Heike Weigand(Ludwig-Maximilians-Universität München), Irina Hüning(University of Lübeck), Urania Kotzaeridou(Heidelberg University), Ingo Borggraefe(Ludwig-Maximilians-Universität München), Sebastian Schröder, Cordula Knopp(RWTH Aachen University), Katharina Vill(Ludwig-Maximilians-Universität München), Melanie Brügger(University of Bern), Luisa Averdunk(Düsseldorf University Hospital), Martje G. Pauly(University of Lübeck), Felix Boschann(University of Cambridge), Markus Bettendorf, Konrad Oexle, Korbinian M. Riedhammer(Boston Children's Hospital), Meino Rohlfs, Georg F. Hoffmann(Heidelberg University), Katrin Hinderhofer, Tobias Bäumer, Christine Makowski(Technical University of Munich), Rebecca Herzog, Katja Lohmann, Martin Krenn, Nazanin Mirza-Schreiber, Reka Kovacs, Wolfgang Müller-Felber, Lilian Kaufmann, Alexander Münchau, Tim Strom, Elisabeth Graf, Fabian Hauck, Britta Hanker, Dominik S. Westphal, Magdalena Danyel(Humboldt-Universität zu Berlin), Ulrich Schatz, Riccardo Berutti(Helmholtz Zentrum München)
RWTH Publications (RWTH Aachen)
January 1, 2025
Cited by 0
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