Assigning a causal role to genetic variants in hypertrophic cardiomyopathy
- PMID: 23424253
- DOI: 10.1161/CIRCGENETICS.111.000032
Assigning a causal role to genetic variants in hypertrophic cardiomyopathy
Comment on
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Formin homology 2 domain containing 3 variants associated with hypertrophic cardiomyopathy.Circ Cardiovasc Genet. 2013 Feb;6(1):10-8. doi: 10.1161/CIRCGENETICS.112.965277. Epub 2012 Dec 19. Circ Cardiovasc Genet. 2013. PMID: 23255317 Free PMC article.
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