Gudrun Nürnberg
- Recessive HYDIN mutations cause primary ciliary dyskinesia without situs abnomalitiesBy Johanna Raidt, Heike Olbrich, Claudius Werner, Niki T. Loges, Nora F. Banki, Amelia Shoemark, Tom Burgoyne, Gabriele Köhler, Josef Schroeder, Gudrun Nürnberg, Peter Nürnberg, Richard Reinhardt and Heymut OmranJohanna Raidt1Klinik fuer Kinder- und Jugendmedizin -Allgemeine Paediatrie, Universitaetsklinikum Muenster, GermanyHeike Olbrich1Klinik fuer Kinder- und Jugendmedizin -Allgemeine Paediatrie, Universitaetsklinikum Muenster, GermanyClaudius Werner1Klinik fuer Kinder- und Jugendmedizin -Allgemeine Paediatrie, Universitaetsklinikum Muenster, GermanyNiki T. Loges1Klinik fuer Kinder- und Jugendmedizin -Allgemeine Paediatrie, Universitaetsklinikum Muenster, GermanyNora F. Banki2Department of Pediatrics, Semmelweis University, Budapest, HungaryAmelia Shoemark3Electron Microscopy Unit, Royal Brompton Hospital, London, United KingdomTom Burgoyne3Electron Microscopy Unit, Royal Brompton Hospital, London, United KingdomGabriele Köhler4Department of Pathology, Universitaetsklinikum Muenster, GermanyJosef Schroeder5Department of Pathology, University of Regensburg, GermanyGudrun Nürnberg6Institute for Genetics, Cologne Center for Genomics, Cologne, GermanyPeter Nürnberg6Institute for Genetics, Cologne Center for Genomics, Cologne, GermanyRichard Reinhardt7Genome Centre Cologne, MPI for Plant Breeding Research, Cologne, GermanyHeymut Omran1Klinik fuer Kinder- und Jugendmedizin -Allgemeine Paediatrie, Universitaetsklinikum Muenster, Germany
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