Evaluation of non-synonymous NPPA single nucleotide polymorphisms in atrial fibrillation

AIMS: Atrial fibrillation (AF), the most common sustained cardiac arrhythmia, is an important cause of morbidity and mortality. A genetic mutation in the NPPA gene, which encodes the atrial natriuretic peptide, has been identified as the putative causative factor in a family with an autosomal domina...

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Bibliografische gegevens
Hoofdauteurs: Roberts, Jason D., Davies, Robert W., Lubitz, Steven A., Thibodeau, Isabelle L., Nery, Pablo B., Birnie, David H., Benjamin, Emelia J., Lemery, Robert, Ellinor, Patrick T., Gollob, Michael H.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Oxford University Press 2010
Onderwerpen:
Clinical Research
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2910603/
https://ncbi.nlm.nih.gov/pubmed/20543198
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/europace/euq161
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