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

Author: 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  

Publisher: Informa Healthcare

ISSN: 0785-3890

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

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content