articles: Association of An Intronic, but Not Any Exonic, FRMD4B Sequence Variant and Heart Failure

Common forms of heart failure (HF) exhibit familial clustering, but specific genetic risk factors have been challenging to identify. A recent single‐nucleotide polymorphism (SNP) microarray study implicated a locus within an intron of FRMD4B in Caucasian HF. Here, we used next‐generation resequencin...

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Detalhes bibliográficos
Main Authors: Matkovich, Scot J., Van Booven, Derek J., Cappola, Thomas P., Dorn II, Gerald W.
Formato: Artigo
Idioma:Inglês
Publicado em: Blackwell Publishing Inc 2010
Assuntos:
Research Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2925316/
https://ncbi.nlm.nih.gov/pubmed/20718813
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1752-8062.2010.00220.x
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