Mikael Koponen

Years Active: 2018-2020
Publications (10 Years): 2

This page only lists publications with an associated author ORCID identifier.

Publications

Mikael Koponen, Annukka Marjamaa, Annukka M Tuiskula, Matti Viitasalo, Terhi Nallinmaa-Luoto, Jaakko T Leinonen, Elisabeth Widen, Lauri Toivonen, Kimmo Kontula, Heikki Swan
Genealogy and clinical course of catecholaminergic polymorphic ventricular tachycardia caused by the ryanodine receptor type 2 P2328S mutation. PloS one 15 (12) (2020)
Mikael Koponen, Aki S Havulinna, Annukka Marjamaa, Annukka M Tuiskula, Veikko Salomaa, Päivi J Laitinen-Forsblom, Kirsi Piippo, Lauri Toivonen, Kimmo Kontula, Matti Viitasalo, Heikki Swan
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. BMC medical genetics 19 (1) (2018)

Mikael Koponen.css-eqlu8i{font-size:small;padding-left:4px;}