A new common mutation in the cardiac beta-myosin heavy chain gene in Finnish patients with hypertrophic cardiomyopathy-Reference-Cited by-同舟云学术

A new common mutation in the cardiac beta-myosin heavy chain gene in Finnish patients with hypertrophic cardiomyopathy

Published:2014-06-03 Issue:6 Volume:46 Page:424-429
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,Kärkkäinen Satu,Peuhkurinen Keijo,Nieminen Markku S.,Laakso Markku,Kuusisto Johanna,

Publisher

Informa UK Limited

Subject

General Medicine

Link

http://www.tandfonline.com/doi/pdf/10.3109/07853890.2014.912834

Reference51 articles.

1. Genetics of Hypertrophic Cardiomyopathy After 20 Years

2. Clinical Features and Outcome of Hypertrophic Cardiomyopathy Associated With Triple Sarcomere Protein Gene Mutations

3. Double or compound sarcomere mutations in hypertrophic cardiomyopathy: A potential link to sudden death in the absence of conventional risk factors

4. A high risk phenotype of hypertrophic cardiomyopathy associated with a compound genotype of two mutated β-myosin heavy chain genes

5. Mutations in the cardiac myosin-binding protein C gene are the predominant cause of familial hypertrophic cardiomyopathy in eastern Finland

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