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Autor:
Morten Krogh Christiansen, Kasper Kjær-Sørensen, Natacha C. Clavsen, Sven Dittmann, Maja Fuhlendorff Jensen, Halvor Østerby Guldbrandsen, Lisbeth Nørum Pedersen, Rikke Hasle Sørensen, Dorte Launholt Lildballe, Klara Müller, Patrick Müller, Kira Vogel, Boris Rudic, Martin Borggrefe, Claus Oxvig, Christian Aalkjær, Eric Schulze-Bahr, Vladimir Matchkov, Henning Bundgaard, Henrik Kjærulf Jensen
Publikováno v:
Christiansen, M K, Kjær-Sørensen, K, Clavsen, N C, Dittmann, S, Jensen, M F, Guldbrandsen, H Ø, Pedersen, L N, Sørensen, R H, Lildballe, D L, Müller, K, Müller, P, Vogel, K, Rudic, B, Borggrefe, M, Oxvig, C, Aalkjær, C, Schulze-Bahr, E, Matchkov, V, Bundgaard, H & Jensen, H K 2023, ' Genetic analysis identifies the SLC4A3 anion exchanger as a major gene for short QT syndrome ', Heart Rhythm . https://doi.org/10.1016/j.hrthm.2023.02.010
BACKGROUND: A variant in the SLC4A3 anion exchanger has been identified as a novel cause of short QT syndrome (SQTS), but the clinical importance of SLC4A3as a cause of SQTS or sudden cardiac death remains unknown.OBJECTIVE: The purpose of this study