Search Results - Suursalmi, P

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    P6325JPH2 p.(Thr161Lys) is a Finnish founder mutation associating to hypertrophic cardiomyopathy with or without systolic heart failure and conduction abnormalities

    P6325JPH2 p.(Thr161Lys) is a Finnish founder mutation associating to hypertrophic cardiomyopathy with or without systolic heart failure and conduction abnormalities by Koskenvuo, J W, Leivo, K, Vanninen, S, Seppala, E H, Aalto-Setala, K, Pitkanen, O, Suursalmi, P, Annala, A.-P, Anttila, I, Alastalo, T.-P, Myllykangas, S, Helio, T H

    Published in European heart journal
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