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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...
में बचाया:
| मुख्य लेखकों: | , , , |
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| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
Blackwell Publishing Inc
2010
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| विषय: | |
| ऑनलाइन पहुंच: | 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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