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

Authors

  • Maximilian G. Posch,

    1. Charité—Universitätsmedizin Berlin, Cardiology at Campus Buch and Helios-Klinikum Berlin-Buch and Max-Delbrück Center for Molecular Medicine, Berlin, Germany
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  • Andreas Perrot,

    1. Charité—Universitätsmedizin Berlin, Cardiology at Campus Buch and Helios-Klinikum Berlin-Buch and Max-Delbrück Center for Molecular Medicine, Berlin, Germany
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  • Katharina Schmitt,

    1. German Heart Institute Berlin, Department of Congenital Heart Disease and Pediatric Cardiology, Berlin, Germany
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  • Sebastian Mittelhaus,

    1. Charité—Universitätsmedizin Berlin, Biomedical Research Center, Berlin, Germany
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  • Eva-Maria Esenwein,

    1. German Heart Institute Berlin, Department of Congenital Heart Disease and Pediatric Cardiology, Berlin, Germany
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  • Brigitte Stiller,

    1. German Heart Institute Berlin, Department of Congenital Heart Disease and Pediatric Cardiology, Berlin, Germany
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  • Christian Geier,

    1. Charité—Universitätsmedizin Berlin, Cardiology at Campus Buch and Helios-Klinikum Berlin-Buch and Max-Delbrück Center for Molecular Medicine, Berlin, Germany
    2. Charité—Universitätsmedizin Berlin, Cardiology at Campus Virchow Klinikum, Berlin, Germany
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  • Rainer Dietz,

    1. Charité—Universitätsmedizin Berlin, Cardiology at Campus Buch and Helios-Klinikum Berlin-Buch and Max-Delbrück Center for Molecular Medicine, Berlin, Germany
    2. Charité—Universitätsmedizin Berlin, Cardiology at Campus Virchow Klinikum, Berlin, Germany
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  • Reinhard Geßner,

    1. Charité—Universitätsmedizin Berlin, Biomedical Research Center, Berlin, Germany
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  • Cemil Özcelik,

    Corresponding author
    1. Charité—Universitätsmedizin Berlin, Cardiology at Campus Buch and Helios-Klinikum Berlin-Buch and Max-Delbrück Center for Molecular Medicine, Berlin, Germany
    • Charité Campus Buch, FVK (Haus 129) CardioGenetic Laboratory, Wiltbergstrasse 50, 13125 Berlin, Germany.
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  • Felix Berger

    1. German Heart Institute Berlin, Department of Congenital Heart Disease and Pediatric Cardiology, Berlin, Germany
    2. Charité—Universitätsmedizin Berlin, Otto-Heubner Centrum at Campus Virchow Klinikum, Berlin, Germany
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  • 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.

No abstract is available for this article.

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