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Kcne3 deletion initiates extracardiac arrhythmogenesis in mice

Mutations in the human KCNE3 potassium channel ancillary subunit gene are associated with life-threatening ventricular arrhythmias. Most genes underlying inherited cardiac arrhythmias, including KCNE3, are not exclusively expressed in the heart, suggesting potentially complex disease etiologies. Her...

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Bibliografiset tiedot
Päätekijät: Hu, Zhaoyang, Crump, Shawn M., Anand, Marie, Kant, Ritu, Levi, Roberto, Abbott, Geoffrey W.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Federation of American Societies for Experimental Biology 2014
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Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3898654/
https://ncbi.nlm.nih.gov/pubmed/24225147
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1096/fj.13-241828
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