Prevalence and spectrum of mutations in a cohort of 192 unrelated patients with hypertrophic cardiomyopathy

Author:

Millat Gilles,Bouvagnet Patrice,Chevalier Philippe,Dauphin Claire,Simon Jouk Pierre,Da Costa Antoine,Prieur Fabienne,Bresson Jean-Luc,Faivre Laurence,Eicher Jean-Christophe,Chassaing Nicolas,Crehalet Hervé,Porcher Raphael,Rodriguez-Lafrasse Claire,Rousson Robert

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference22 articles.

1. Genetic background in patients with acute myocardial infarction;Aoki;Jpn. Heart J.,2001

2. Controlling the false discovery rate: a new and powerful approach to multiple testing;Benjamini;J. Royal Stat. Soc. Series. B. Stat. Methodol.,1995

3. Genetics of hypertrophic cardiomyopathy: one, two, or more diseases?;Bos;Curr. Opin. Cardiol.,2007

4. Clinical features and prognostic implications of familial hypertrophic cardiomyopathy related to the cardiac myosin-binding protein C gene;Charron;Circulation,1998

5. Adverse events in families with hypertrophic or dilated cardiomyopathy and mutations in the MYBPC3 gene;Ehlermann;BMC Med. Genet.,2008

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