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-Reference-Cited by-同舟云学术

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

Published:2012-04-02 Issue:1 Volume:45 Page:85-90
ISSN:0785-3890
Container-title:Annals of Medicine
language:en
Short-container-title:Annals of Medicine

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 UK Limited

Subject

General Medicine

Link

http://www.tandfonline.com/doi/pdf/10.3109/07853890.2012.671534

Reference26 articles.

1. Mutation Type Is Not Clinically Useful in Predicting Prognosis in Hypertrophic Cardiomyopathy

2. Genetics and Clinical Destiny: Improving Care in Hypertrophic Cardiomyopathy

3. Hypertrophic Cardiomyopathy

4. Mutation spectrum in a large cohort of unrelated consecutive patients with hypertrophic cardiomyopathy

5. Prevalence and Spectrum of Thin Filament Mutations in an Outpatient Referral Population With Hypertrophic Cardiomyopathy

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