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Year | Number of Results |
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1999 | 1 |
2008 | 2 |
2024 | 0 |
PubMed (cited) for id: 612955
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alpha-1-syntrophin mutation and the long-QT syndrome: a disease of sodium channel disruption.
Circ Arrhythm Electrophysiol. 2008 Aug;1(3):193-201. doi: 10.1161/CIRCEP.108.769224.
Circ Arrhythm Electrophysiol. 2008.
PMID: 19684871
Free PMC article.
Syntrophin mutation associated with long QT syndrome through activation of the nNOS-SCN5A macromolecular complex.
Ueda K, Valdivia C, Medeiros-Domingo A, Tester DJ, Vatta M, Farrugia G, Ackerman MJ, Makielski JC.
Ueda K, et al.
Proc Natl Acad Sci U S A. 2008 Jul 8;105(27):9355-60. doi: 10.1073/pnas.0801294105. Epub 2008 Jun 30.
Proc Natl Acad Sci U S A. 2008.
PMID: 18591664
Free PMC article.
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Novel KCNQ1 and HERG missense mutations in Dutch long-QT families.
Jongbloed RJ, Wilde AA, Geelen JL, Doevendans P, Schaap C, Van Langen I, van Tintelen JP, Cobben JM, Beaufort-Krol GC, Geraedts JP, Smeets HJ.
Jongbloed RJ, et al.
Hum Mutat. 1999;13(4):301-10. doi: 10.1002/(SICI)1098-1004(1999)13:4<301::AID-HUMU7>3.0.CO;2-V.
Hum Mutat. 1999.
PMID: 10220144
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