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Year | Number of Results |
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2004 | 1 |
2005 | 2 |
2009 | 1 |
2012 | 1 |
2024 | 0 |
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Page 1
Paralogous annotation of disease-causing variants in long QT syndrome genes.
Hum Mutat. 2012 Aug;33(8):1188-1191. doi: 10.1002/humu.22114. Epub 2012 Jun 7.
Hum Mutat. 2012.
PMID: 22581653
Free PMC article.
A novel SCN5A mutation manifests as a malignant form of long QT syndrome with perinatal onset of tachycardia/bradycardia.
Chang CC, Acharfi S, Wu MH, Chiang FT, Wang JK, Sung TC, Chahine M.
Chang CC, et al.
Cardiovasc Res. 2004 Nov 1;64(2):268-78. doi: 10.1016/j.cardiores.2004.07.007.
Cardiovasc Res. 2004.
PMID: 15485686
Item in Clipboard
Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing.
Tester DJ, Will ML, Haglund CM, Ackerman MJ.
Tester DJ, et al.
Heart Rhythm. 2005 May;2(5):507-17. doi: 10.1016/j.hrthm.2005.01.020.
Heart Rhythm. 2005.
PMID: 15840476
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Gene sequencing in neonates and infants with the long QT syndrome.
Shim SH, Ito M, Maher T, Milunsky A.
Shim SH, et al.
Genet Test. 2005 Winter;9(4):281-4. doi: 10.1089/gte.2005.9.281.
Genet Test. 2005.
PMID: 16379539
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Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic test.
Kapplinger JD, Tester DJ, Salisbury BA, Carr JL, Harris-Kerr C, Pollevick GD, Wilde AA, Ackerman MJ.
Kapplinger JD, et al.
Heart Rhythm. 2009 Sep;6(9):1297-303. doi: 10.1016/j.hrthm.2009.05.021. Epub 2009 Jun 23.
Heart Rhythm. 2009.
PMID: 19716085
Free PMC article.
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