Genealogy and clinical course of catecholaminergic polymorphic ventricular tachycardia caused by the ryanodine receptor type 2 P2328S mutation

por Koponen, Mikael, Marjamaa, Annukka, Tuiskula, Annukka M., Viitasalo, Matti, Nallinmaa-Luoto, Terhi, Leinonen, Jaakko T., Widen, Elisabeth, Toivonen, Lauri, Kontula, Kimmo, Swan, Heikki
Publicado 2020

Clinical and molecular genetic risk determinants in adult long QT syndrome type 1 and 2 patients: Koponen et al. Follow-up of adult LQTS patients

por Koponen, Mikael, Havulinna, Aki S., Marjamaa, Annukka, Tuiskula, Annukka M., Salomaa, Veikko, Laitinen-Forsblom, Päivi J., Piippo, Kirsi, Toivonen, Lauri, Kontula, Kimmo, Viitasalo, Matti, Swan, Heikki
Publicado 2018

An actionable KCNH2 Long QT Syndrome variant detected by sequence and haplotype analysis in a population research cohort

por Kerr, Shona M., Klaric, Lucija, Halachev, Mihail, Hayward, Caroline, Boutin, Thibaud S., Meynert, Alison M., Semple, Colin A., Tuiskula, Annukka M., Swan, Heikki, Santoyo-Lopez, Javier, Vitart, Veronique, Haley, Chris, Dean, John, Miedzybrodzka, Zosia, Aitman, Timothy J., Wilson, James F.
Publicado 2019