Founder mutations in hypertrophic cardiomyopathy patients in the Netherlands*-Reference-Cited by-同舟云学术

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Founder mutations in hypertrophic cardiomyopathy patients in the Netherlands*

Published:2014 Issue: Volume: Page:37-42
ISSN:
Container-title:De Nederlandse gezondheidszorg
language:
Short-container-title:

Author:

Christiaans I.,Nannenberg E.A.,Dooijes D.,Jongbloed R.J.E.,Michels M.,Postema P.G.,Majoor-Krakauer D.,van den Wijngaard A.,Mannens M.M.A.M.,van Tintelen J.P.,van Langen I.M.,Wilde A.A.M.

Publisher

Bohn Stafleu van Loghum

Link

http://link.springer.com/content/pdf/10.1007/978-90-368-0705-0_6

Reference80 articles.

1. Maron BJ, Gardin JM, Flack JM, Gidding SS, Kurosaki TT, Bild DE. Prevalence of hypertrophic cardiomyopathy in a general population of young adults. Echocardiographic analysis of 4111 subjects in the CARDIA Study. Coronary Artery Risk Development in (Young) Adults. Circulation. 1995;92:785-9.

2. Morita H, Larson MG, Barr SC et al. Single-gene mutations and increased left ventricular wall thickness in the community: the Framingham Heart Study. Circulation. 2006;113:2697-705.

3. Teare D. Asymmetrical hypertrophy of the heart in young adults. Br Heart J. 1958;20:1-8.

4. Watkins H, Ashrafian H, McKenna WJ. The genetics of hypertrophic cardiomyopathy: Teare redux. Heart. 2008;94:1264-8.

5. Elliott P, Andersson B, Arbustini E, et al. Classification of the cardiomyopathies: a position statement from the European Society Of Cardiology Working Group on Myocardial and Pericardial Diseases. Eur Heart J. 2008;29:270-6.

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