Long QT Interval in Turner Syndrome – A High Prevalence of LQTS Gene Mutations

por Trolle, Christian, Mortensen, Kristian H., Pedersen, Lisbeth N., Berglund, Agnethe, Jensen, Henrik K., Andersen, Niels H., Gravholt, Claus H.
Publicado 2013

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

por Thorsen, Kasper, Dam, Vibeke S., Kjaer-Sorensen, Kasper, Pedersen, Lisbeth N., Skeberdis, V. Arvydas, Jurevičius, Jonas, Treinys, Rimantas, Petersen, Ida M. B. S., Nielsen, Morten S., Oxvig, Claus, Morth, J. Preben, Matchkov, Vladimir V., Aalkjær, Christian, Bundgaard, Henning, Jensen, Henrik K.
Publicado 2017

Mutations in Danish patients with long QT syndrome and the identification of a large founder family with p.F29L in KCNH2

por Christiansen, Michael, Hedley, Paula L, Theilade, Juliane, Stoevring, Birgitte, Leren, Trond P, Eschen, Ole, Sørensen, Karina M, Tybjærg-Hansen, Anne, Ousager, Lilian B, Pedersen, Lisbeth N, Frikke-Schmidt, Ruth, Aidt, Frederik H, Hansen, Michael G, Hansen, Jim, Bloch Thomsen, Poul E, Toft, Egon, Henriksen, Finn L, Bundgaard, Henning, Jensen, Henrik K, Kanters, Jørgen K
Publicado 2014