POPDC2 a novel susceptibility gene for conduction disorders

Despite recent progress in the understanding of cardiac ion channel function and its role in inherited forms of ventricular arrhythmias, the molecular basis of cardiac conduction disorders often remains unresolved. We aimed to elucidate the genetic background of familial atrioventricular block (AVB)...

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Veröffentlicht in:	Journal of molecular and cellular cardiology 2020-08, Vol.145, p.74-83
Hauptverfasser:	Rinné, Susanne, Ortiz-Bonnin, Beatriz, Stallmeyer, Birgit, Kiper, Aytug K., Fortmüller, Lisa, Schindler, Roland F.R., Herbort-Brand, Ursula, Kabir, Nashitha S., Dittmann, Sven, Friedrich, Corinna, Zumhagen, Sven, Gualandi, Francesca, Selvatici, Rita, Rapezzi, Claudio, Arbustini, Eloisa, Ferlini, Alessandra, Fabritz, Larissa, Schulze-Bahr, Eric, Brand, Thomas, Decher, Niels
Format:	Artikel
Sprache:	eng
Schlagworte:	Arrhythmia Atrioventricular block Ion channels Whole exome sequencing
Online-Zugang:	Volltext
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