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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
Jääskeläinen, Pertti, Heliö, Tiina, Aalto-Setälä, Katriina, Kaartinen, Maija, Ilveskoski, Erkki, Hämäläinen, Liisa, Melin, John, Nieminen, Markku S., Laakso, Markku, Kuusisto, Johanna, Kervinen, HelenVolume:
45
Language:
english
Journal:
Annals of Medicine
DOI:
10.3109/07853890.2012.671534
Date:
February, 2013
File:
PDF, 294 KB
english, 2013