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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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2003 | 1 |
2010 | 1 |
2011 | 2 |
2024 | 0 |
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Page 1
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
Mutations in sodium channel β-subunit SCN3B are associated with early-onset lone atrial fibrillation.
Olesen MS, Jespersen T, Nielsen JB, Liang B, Møller DV, Hedley P, Christiansen M, Varró A, Olesen SP, Haunsø S, Schmitt N, Svendsen JH.
Olesen MS, et al.
Cardiovasc Res. 2011 Mar 1;89(4):786-93. doi: 10.1093/cvr/cvq348. Epub 2010 Nov 4.
Cardiovasc Res. 2011.
PMID: 21051419
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Multiple arrhythmic syndromes in a newborn, owing to a novel mutation in SCN5A.
Calloe K, Schmitt N, Grubb S, Pfeiffer R, David JP, Kanter R, Cordeiro JM, Antzelevitch C.
Calloe K, et al.
Can J Physiol Pharmacol. 2011 Oct;89(10):723-36. doi: 10.1139/y11-070. Epub 2011 Sep 6.
Can J Physiol Pharmacol. 2011.
PMID: 21895525
Free PMC article.
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