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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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2000 | 1 |
2009 | 1 |
2014 | 1 |
2024 | 0 |
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Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2.
Circulation. 2000 Sep 5;102(10):1178-85. doi: 10.1161/01.cir.102.10.1178.
Circulation. 2000.
PMID: 10973849
The genetic basis of long QT and short QT syndromes: a mutation update.
Hedley PL, Jørgensen P, Schlamowitz S, Wangari R, Moolman-Smook J, Brink PA, Kanters JK, Corfield VA, Christiansen M.
Hedley PL, et al.
Hum Mutat. 2009 Nov;30(11):1486-511. doi: 10.1002/humu.21106.
Hum Mutat. 2009.
PMID: 19862833
Review.
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Position of premature termination codons determines susceptibility of hERG mutations to nonsense-mediated mRNA decay in long QT syndrome.
Gong Q, Stump MR, Zhou Z.
Gong Q, et al.
Gene. 2014 Apr 15;539(2):190-7. doi: 10.1016/j.gene.2014.02.012. Epub 2014 Feb 13.
Gene. 2014.
PMID: 24530480
Free PMC article.
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