Two founder mutations in the alpha-tropomyosin and the cardiac myosin-binding protein C genes are common causes of hypertrophic cardiomyopathy in the Finnish population
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| Description | scientific article published on 2 April 2012 |
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author: Pertti Jääskeläinen Maija A Kaartinen Johanna Kuusisto Mikko Pietilä Katriina Aalto-Setälä Liisa Hämäläinen Markku Laakso Erkki Ilveskoski Tiina Heliö |
| Publication date | April 2, 2012 |
| Language | English |
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