Editorial
doi: 10.1016/j.jacc.2009.12.025.
A glimpse into multigene rare variant genetics: triple mutations in hypertrophic cardiomyopathy
- PMID: 20359595
- PMCID: PMC2915403
- DOI: 10.1016/j.jacc.2009.12.025
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Editorial
A glimpse into multigene rare variant genetics: triple mutations in hypertrophic cardiomyopathy
J Am Coll Cardiol.
.
No abstract available
Comment on
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Clinical features and outcome of hypertrophic cardiomyopathy associated with triple sarcomere protein gene mutations.J Am Coll Cardiol. 2010 Apr 6;55(14):1444-53. doi: 10.1016/j.jacc.2009.11.062. J Am Coll Cardiol. 2010. PMID: 20359594
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References
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- Girolami F, Ho C, Semsarian C, et al. Clinical features and outcome of hypertrophic cardiomyopathy associatied with triple sarcomere protein gene mutations. J Am Coll Cardiol. 2009 in press. - PubMed
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- Van Driest SL, Vasile VC, Ommen SR, et al. Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy. J Am Coll Cardiol. 2004;44:1903–1910. - PubMed
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- Richard P, Charron P, Carrier L, et al. Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy. Circulation. 2003;107:2227–2232. - PubMed
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