Presenilin 2 deficiency causes a mild pulmonary phenotype and no changes in amyloid precursor protein processing but enhances the embryonic lethal phenotype of presenilin 1 deficiency
An Herreman(Vlaams Instituut voor Biotechnologie), Bart De Strooper(VIB-KU Leuven Center for Brain & Disease Research), Wim Annaert(VIB-KU Leuven Center for Microbiology), Lutgarde Serneels(VIB-KU Leuven Center for Brain & Disease Research), Danny Huylebroeck(Erasmus MC), Paul Säftig(Christian-Albrechts-Universität zu Kiel), Lieve Umans(Vlaams Instituut voor Biotechnologie), Hugo Vanderstichele(ADx NeuroSciences), Philippe Cupers(Vlaams Instituut voor Biotechnologie), Vincent Schrijvers(Vlaams Instituut voor Biotechnologie), Ralf Dressel(Universitätsmedizin Göttingen), Veerle Baekelandt(Allen Institute for Brain Science), Katleen Craessaerts(VIB-KU Leuven Center for Brain & Disease Research), Frédéric Checler(Centre National de la Recherche Scientifique), Dieter Hartmann(University of Bonn), Fred Van Leuven(KU Leuven), An Zwijsen(KU Leuven)
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