S. Weckström

DSP p.(Thr2104Glnfs*12) variant presents variably with early onset severe arrhythmias and left ventricular cardiomyopathy

T. Heliö, S. Myllykangas, J. Koskenvuo, 2020, BMC Medical Genetics.

A novel desmoplakin mutation causes dilated cardiomyopathy with palmoplantar keratoderma as an early clinical sign

T. Heliö, K. Kettunen, A. Ranki, 2022, Journal of the European Academy of Dermatology and Venereology : JEADV.

MYH7 Genotype–Phenotype Correlation in a Cohort of Finnish Patients

C. Vasilescu, T. Ojala, T. Heliö, 2022, Cardiogenetics.

Timing of pacemaker and ICD implantation in LMNA mutation carriers

K. Nikus, H. Parikka, S. Weckström, 2021, Open Heart.

Biallelic loss-of-function in NRAP is a cause of recessive dilated cardiomyopathy.

T. Ojala, M. Gentile, S. Ahonen, 2021, PloS one.

GRINL1A Complex Transcription Unit Containing GCOM1, MYZAP, and POLR2M Genes Associates with Fully Penetrant Recessive Dilated Cardiomyopathy

K. Nikus, M. Gentile, S. Ahonen, 2021, Frontiers in Genetics.

DSP c.6310delA p.(Thr2104Glnfs*12) associates with arrhythmogenic cardiomyopathy, increased trabeculation, curly hair, and palmoplantar keratoderma

T. Heliö, J. Koskenvuo, M. Holmström, 2023, Frontiers in Cardiovascular Medicine.