Mikael Koponen

2PUBLICATIONS
1CO-AUTHORS
Cancer genetics
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Publications (2)

|Dec 14, 2020
Genealogy and clinical course of catecholaminergic polymorphic ventricular tachycardia caused by the ryanodine receptor type 2 P2328S mutation.

Mikael Koponen, Annukka Marjamaa, Annukka M Tuiskula

|Apr 07, 2018
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.

Mikael Koponen, Aki S Havulinna, Annukka Marjamaa

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Frequent Collaborators

1 joint publications

Annukka M Tuiskula