Mutations in GATA4, NKX2.5, CRELD1, and BMP4 are infrequently found in patients with congenital cardiac septal defects

Abstract

American Journal of Medical Genetics Part AVolume 146A, Issue 2 p. 251-253 Research Letter Mutations in GATA4, NKX2.5, CRELD1, and BMP4 are infrequently found in patients with congenital cardiac septal defects†‡ Maximilian G. Posch, Maximilian G. Posch Charité—Universitätsmedizin Berlin, Cardiology at Campus Buch and Helios-Klinikum Berlin-Buch and Max-Delbrück Center for Molecular Medicine, Berlin, GermanySearch for more papers by this authorAndreas Perrot, Andreas Perrot Charité—Universitätsmedizin Berlin, Cardiology at Campus Buch and Helios-Klinikum Berlin-Buch and Max-Delbrück Center for Molecular Medicine, Berlin, GermanySearch for more papers by this authorKatharina Schmitt, Katharina Schmitt German Heart Institute Berlin, Department of Congenital Heart Disease and Pediatric Cardiology, Berlin, GermanySearch for more papers by this authorSebastian Mittelhaus, Sebastian Mittelhaus Charité—Universitätsmedizin Berlin, Biomedical Research Center, Berlin, GermanySearch for more papers by this authorEva-Maria Esenwein, Eva-Maria Esenwein German Heart Institute Berlin, Department of Congenital Heart Disease and Pediatric Cardiology, Berlin, GermanySearch for more papers by this authorBrigitte Stiller, Brigitte Stiller German Heart Institute Berlin, Department of Congenital Heart Disease and Pediatric Cardiology, Berlin, GermanySearch for more papers by this authorChristian Geier, Christian Geier Charité—Universitätsmedizin Berlin, Cardiology at Campus Buch and Helios-Klinikum Berlin-Buch and Max-Delbrück Center for Molecular Medicine, Berlin, Germany Charité—Universitätsmedizin Berlin, Cardiology at Campus Virchow Klinikum, Berlin, GermanySearch for more papers by this authorRainer Dietz, Rainer Dietz Charité—Universitätsmedizin Berlin, Cardiology at Campus Buch and Helios-Klinikum Berlin-Buch and Max-Delbrück Center for Molecular Medicine, Berlin, Germany Charité—Universitätsmedizin Berlin, Cardiology at Campus Virchow Klinikum, Berlin, GermanySearch for more papers by this authorReinhard Geßner, Reinhard Geßner Charité—Universitätsmedizin Berlin, Biomedical Research Center, Berlin, GermanySearch for more papers by this authorCemil Özcelik, Corresponding Author Cemil Özcelik oezcelik@mdc-berlin.de Charité—Universitätsmedizin Berlin, Cardiology at Campus Buch and Helios-Klinikum Berlin-Buch and Max-Delbrück Center for Molecular Medicine, Berlin, GermanyCharité Campus Buch, FVK (Haus 129) CardioGenetic Laboratory, Wiltbergstrasse 50, 13125 Berlin, Germany.Search for more papers by this authorFelix Berger, Felix Berger German Heart Institute Berlin, Department of Congenital Heart Disease and Pediatric Cardiology, Berlin, Germany Charité—Universitätsmedizin Berlin, Otto-Heubner Centrum at Campus Virchow Klinikum, Berlin, GermanySearch for more papers by this author Maximilian G. Posch, Maximilian G. Posch Charité—Universitätsmedizin Berlin, Cardiology at Campus Buch and Helios-Klinikum Berlin-Buch and Max-Delbrück Center for Molecular Medicine, Berlin, GermanySearch for more papers by this authorAndreas Perrot, Andreas Perrot Charité—Universitätsmedizin Berlin, Cardiology at Campus Buch and Helios-Klinikum Berlin-Buch and Max-Delbrück Center for Molecular Medicine, Berlin, GermanySearch for more papers by this authorKatharina Schmitt, Katharina Schmitt German Heart Institute Berlin, Department of Congenital Heart Disease and Pediatric Cardiology, Berlin, GermanySearch for more papers by this authorSebastian Mittelhaus, Sebastian Mittelhaus Charité—Universitätsmedizin Berlin, Biomedical Research Center, Berlin, GermanySearch for more papers by this authorEva-Maria Esenwein, Eva-Maria Esenwein German Heart Institute Berlin, Department of Congenital Heart Disease and Pediatric Cardiology, Berlin, GermanySearch for more papers by this authorBrigitte Stiller, Brigitte Stiller German Heart Institute Berlin, Department of Congenital Heart Disease and Pediatric Cardiology, Berlin, GermanySearch for more papers by this authorChristian Geier, Christian Geier Charité—Universitätsmedizin Berlin, Cardiology at Campus Buch and Helios-Klinikum Berlin-Buch and Max-Delbrück Center for Molecular Medicine, Berlin, Germany Charité—Universitätsmedizin Berlin, Cardiology at Campus Virchow Klinikum, Berlin, GermanySearch for more papers by this authorRainer Dietz, Rainer Dietz Charité—Universitätsmedizin Berlin, Cardiology at Campus Buch and Helios-Klinikum Berlin-Buch and Max-Delbrück Center for Molecular Medicine, Berlin, Germany Charité—Universitätsmedizin Berlin, Cardiology at Campus Virchow Klinikum, Berlin, GermanySearch for more papers by this authorReinhard Geßner, Reinhard Geßner Charité—Universitätsmedizin Berlin, Biomedical Research Center, Berlin, GermanySearch for more papers by this authorCemil Özcelik, Corresponding Author Cemil Özcelik oezcelik@mdc-berlin.de Charité—Universitätsmedizin Berlin, Cardiology at Campus Buch and Helios-Klinikum Berlin-Buch and Max-Delbrück Center for Molecular Medicine, Berlin, GermanyCharité Campus Buch, FVK (Haus 129) CardioGenetic Laboratory, Wiltbergstrasse 50, 13125 Berlin, Germany.Search for more papers by this authorFelix Berger, Felix Berger German Heart Institute Berlin, Department of Congenital Heart Disease and Pediatric Cardiology, Berlin, Germany Charité—Universitätsmedizin Berlin, Otto-Heubner Centrum at Campus Virchow Klinikum, Berlin, GermanySearch for more papers by this author First published: 12 December 2007 https://doi.org/10.1002/ajmg.a.32042Citations: 66 † A. Perrot, K. Schmitt, S. Mittelhaus, C. Özcelik, and F. Berger contributed equally to this work. ‡ How to cite this article: Posch MG, Perrot A, Schmitt K, Mittelhaus S, Esenwein E-M, Stiller B, Geier C, Dietz R, Geßner R, Özcelik C, Berger F. 2007. Mutations in GATA4, NKX2.5, CRELD1, and BMP4 are infrequently found in patients with congenital cardiac septal defects. Am J Med Genet Part A 146A:251–253. Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinked InRedditWechat Citing Literature Volume146A, Issue215 January 2008Pages 251-253 RelatedInformation