Loss-of-activity-mutation in the cardiac chloride-bicarbonate exchanger AE3 causes short QT syndrome

Kasper Thorsen, Vibeke S. Dam, Kasper Kjaer-Sorensen, Lisbeth N. Pedersen, V. Arvydas Skeberdis, Jonas Jurevičius, Rimantas Treinys, Ida M. B. S. Petersen, Morten S. Nielsen, Claus Oxvig, J. Preben Morth, Vladimir V. Matchkov, Christian Aalkjær, Henning Bundgaard and Henrik K. Jensen ()
Additional contact information
Kasper Thorsen: Aarhus University Hospital, Palle Juul-Jensens Boulevard 99
Vibeke S. Dam: Aarhus University
Kasper Kjaer-Sorensen: Aarhus University
Lisbeth N. Pedersen: Aarhus University Hospital, Palle Juul-Jensens Boulevard 99
V. Arvydas Skeberdis: Lithuanian University of Health Sciences
Jonas Jurevičius: Lithuanian University of Health Sciences
Rimantas Treinys: Lithuanian University of Health Sciences
Ida M. B. S. Petersen: University of Copenhagen
Morten S. Nielsen: University of Copenhagen
Claus Oxvig: Aarhus University
J. Preben Morth: University of Oslo
Vladimir V. Matchkov: Aarhus University
Christian Aalkjær: Aarhus University
Henning Bundgaard: National University Hospital, Rigshospitalet, Copenhagen Health Science Partners, University of Copenhagen
Henrik K. Jensen: Aarhus University Hospital

Nature Communications, 2017, vol. 8, issue 1, 1-10

Abstract: Abstract Patients with short QT syndrome (SQTS) may present with syncope, ventricular fibrillation or sudden cardiac death. Six SQTS susceptibility genes, encoding cation channels, explain

Date: 2017
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DOI: 10.1038/s41467-017-01630-0

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