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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2007 | 1 |
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A ubiquitous splice variant and a common polymorphism affect heterologous expression of recombinant human SCN5A heart sodium channels.
Circ Res. 2003 Oct 31;93(9):821-8. doi: 10.1161/01.RES.0000096652.14509.96. Epub 2003 Sep 18.
Circ Res. 2003.
PMID: 14500339
Combination of cardiac conduction disease and long QT syndrome caused by mutation T1620K in the cardiac sodium channel.
Surber R, Hensellek S, Prochnau D, Werner GS, Benndorf K, Figulla HR, Zimmer T.
Surber R, et al.
Cardiovasc Res. 2008 Mar 1;77(4):740-8. doi: 10.1093/cvr/cvm096. Epub 2007 Dec 7.
Cardiovasc Res. 2008.
PMID: 18065446
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Mutations in sodium channel β1- and β2-subunits associated with atrial fibrillation.
Watanabe H, Darbar D, Kaiser DW, Jiramongkolchai K, Chopra S, Donahue BS, Kannankeril PJ, Roden DM.
Watanabe H, et al.
Circ Arrhythm Electrophysiol. 2009 Jun;2(3):268-75. doi: 10.1161/CIRCEP.108.779181. Epub 2009 Mar 6.
Circ Arrhythm Electrophysiol. 2009.
PMID: 19808477
Free PMC article.
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Mexiletine differentially restores the trafficking defects caused by two brugada syndrome mutations.
Moreau A, Keller DI, Huang H, Fressart V, Schmied C, Timour Q, Chahine M.
Moreau A, et al.
Front Pharmacol. 2012 Apr 20;3:62. doi: 10.3389/fphar.2012.00062. eCollection 2012.
Front Pharmacol. 2012.
PMID: 22529811
Free PMC article.
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