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Year | Number of Results |
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1999 | 1 |
2010 | 1 |
2013 | 1 |
2014 | 1 |
2024 | 0 |
PubMed (cited) for id: 613485
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A Kir3.4 mutation causes Andersen-Tawil syndrome by an inhibitory effect on Kir2.1.
Neurology. 2014 Mar 25;82(12):1058-64. doi: 10.1212/WNL.0000000000000239. Epub 2014 Feb 26.
Neurology. 2014.
PMID: 24574546
The phenotype characteristics of type 13 long QT syndrome with mutation in KCNJ5 (Kir3.4-G387R).
Wang F, Liu J, Hong L, Liang B, Graff C, Yang Y, Christiansen M, Olesen SP, Zhang L, Kanters JK.
Wang F, et al.
Heart Rhythm. 2013 Oct;10(10):1500-6. doi: 10.1016/j.hrthm.2013.07.022. Epub 2013 Jul 18.
Heart Rhythm. 2013.
PMID: 23872692
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Identification of a Kir3.4 mutation in congenital long QT syndrome.
Yang Y, Yang Y, Liang B, Liu J, Li J, Grunnet M, Olesen SP, Rasmussen HB, Ellinor PT, Gao L, Lin X, Li L, Wang L, Xiao J, Liu Y, Liu Y, Zhang S, Liang D, Peng L, Jespersen T, Chen YH.
Yang Y, et al.
Am J Hum Genet. 2010 Jun 11;86(6):872-80. doi: 10.1016/j.ajhg.2010.04.017.
Am J Hum Genet. 2010.
PMID: 20560207
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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