Related content

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

By Jääskeläinen Pertti   Heliö Tiina   Aalto-Setälä Katriina   Kaartinen Maija   Ilveskoski Erkki   Hämäläinen Liisa   Melin John   Nieminen Markku S.   Laakso Markku   Kuusisto Johanna     Kervinen Helena   Mustonen Juha   Juvonen Jukka   Niemi Mari   Uusimaa Paavo   Huttunen Matti   Kotila Matti   Pietilä Mikko  

Annals of Medicine, Vol. 45, Iss. 1, 2013-02 ,pp. : 85-90

Informa Healthcare

Access to resources Recommend Favorite

Genetics of hypertrophic cardiomyopathy in eastern Finland: few founder mutations with benign or intermediary phenotypes

By Jääskeläinen Pertti   Miettinen Raija   Kärkkäinen Päivi   Toivonen Lauri   Laakso Markku   Kuusisto Johanna  

Annals of Medicine, Vol. 36, Iss. 1, 2004-01 ,pp. : 23-32

Informa Healthcare

Access to resources Recommend Favorite

Variants in miRNA Regulating Cardiac Growth Are Not a Common Cause of Hypertrophic Cardiomyopathy

By  

Cardiology, Vol. 130, Iss. 3, 2015-01 ,pp. : 137-142

Karger

Access to resources Recommend Favorite

Familial hypertrophic cardiomyopathy caused by a de novo Gly716Arg mutation of the β-myosin heavy chain

By  

Cardiology in the Young, Vol. 27, Iss. 3, 2016-05 ,pp. : 467-472

Cambridge University Press

Access to resources Recommend Favorite

Phenotypic Variation of Familial Hypertrophic Cardiomyopathy Caused by the Phe¹¹⁰→Ile Mutation in Cardiac Troponin T

By  

Cardiology, Vol. 93, Iss. 3, 2000-08 ,pp. : 155-162

Karger

Access to resources Recommend Favorite