Clinical Research in Cardiology

, Volume 95, Issue 9, pp 499–503

Familial congenital heart disease, progressive atrioventricular block and the cardiac homeobox transcription factor gene NKX2.5:

identification of a novel mutation
  • Kai König
  • Joachim C. Will
  • Felix Berger
  • Dominik Müller
  • D. Woodrow Benson
CLINICAL CORRESPONDENCE

DOI: 10.1007/s00392-006-0412-9

Cite this article as:
König, K., Will, J.C., Berger, F. et al. Clin Res Cardiol (2006) 95: 499. doi:10.1007/s00392-006-0412-9

Copyright information

© Steinkopff-Verlag 2006

Authors and Affiliations

  • Kai König
    • 1
    • 2
  • Joachim C. Will
    • 1
  • Felix Berger
    • 1
  • Dominik Müller
    • 1
  • D. Woodrow Benson
    • 3
  1. 1.Otto-Heubner-Centrum für Kinder- und JugendmedizinCharité Campus Virchow KlinikumBerlinGermany
  2. 2.Mercy Hospital for WomenDepartment of PaediatricsHeidelberg/Melbourne (VIC)Australia
  3. 3.Cincinnati Children’s Hospital Medical CenterCincinnatiUSA