The missense variant p.(Gly482Arg) in HCN4 is responsible for fetal tachy-bradycardia syndrome

HeartRhythm Case Rep. 2020 Mar 20;6(6):352-356. doi: 10.1016/j.hrcr.2020.03.003. eCollection 2020 Jun.

¹ Institute of Preventive Pediatrics, Technical University of Munich, and Department of Pediatric Cardiology and Adult Congenital Heart Disease Munich, German Heart Center Munich, Munich, Germany.
² Institute of Human Genetics, Technical University of Munich, Munich, Germany.
³ Institute of Human Genetics, Helmholtz Zentrum Munich, Neuherberg, Germany.
⁴ Department of Electrophysiology, German Heart Center Munich, Munich, Germany.
⁵ Department of Medical Physics, University of Wisconsin-Madison, Madison, Wisconsin.
⁶ Department of Pediatrics, Division of Cardiology Herma Heart Institute, Children's Wisconsin, Milwaukee, Wisconsin.

No abstract available

Keywords: Arrhythmia; De novo; Fetal bradycardia; HCN4; Prenatal.

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