Samuel Myllykangas

Person

Latest publications

  1. Relevance of Titin Missense and Non-Frameshifting Insertions/Deletions Variants in Dilated Cardiomyopathy

    Akinrinade, O., Heliö, T., Deprez, R. H. L., Jongbloed, J. D. H., Boven, L. G., van den Berg, M. P., Pinto, Y. M., Alastalo, T-P., Myllykangas, S., van Spaendonck-Zwarts, K., van Tintelen, J. P., van der Zwaag, P. A. & Koskenvuo, J., 11 Mar 2019, In : Scientific Reports. 9, 9 p., 4093.

    Research output: Contribution to journalArticleScientificpeer-review

  2. Heterozygous junctophilin-2 (JPH2) p. (Thr161Lys) is a monogenic cause for HCM with heart failure

    Vanninen, S. U. M., Leivo, K., Seppälä, E. H., Aalto-Setälä, K., Pitkänen, O., Suursalmi, P., Annala, A-P., Anttila, I., Alastalo, T-P., Myllykangas, S., Heliö, T. M. & Koskenvuo, J. W., 20 Sep 2018, In : PLoS One. 13, 9, 14 p., 0203422.

    Research output: Contribution to journalArticleScientificpeer-review

  3. Case reports of two pedigrees with recessive arrhythmogenic right ventricular cardiomyopathy associated with homozygous Thr335Ala variant in DSG2

    Qadri, S., Anttonen, O., Viikila, J., Seppala, E. H., Myllykangas, S., Alastalo, T-P., Holmstrom, M., Helio, T. & Koskenvuo, J. W., 17 Aug 2017, In : BMC Medical Genetics. 18, 9 p., 86.

    Research output: Contribution to journalArticleScientificpeer-review

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