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Query Trace: Seizures and KCNH2[original query]

Genome sequencing in a genetically elusive multigenerational long QT syndrome pedigree identifies a novel LQT2-causative deeply intronic KCNH2 variant. Heart rhythm 2022 2 19 (6): 998-1007. Tobert Kathryn E, Tester David J, Zhou Wei, Haglund-Turnquist Carla M, Giudicessi John R, Ackerman Michael Similar articles in PubMed
Genetic biomarkers for the risk of seizures in long QT syndrome. Neurology 2016 Oct 87 (16): 1660-1668. Auerbach David S, McNitt Scott, Gross Robert A, Zareba Wojciech, Dirksen Robert T, Moss Arthur Similar articles in PubMed
Prevalence and spectrum of large deletions or duplications in the major long QT syndrome-susceptibility genes and implications for long QT syndrome genetic testing. The American journal of cardiology 2010 Oct 106 (8): 1124-8. Tester David J, Benton Amber J, Train Laura, Deal Barbara, Baudhuin Linnea M, Ackerman Michael Similar articles in PubMed
DHPLC analysis of potassium ion channel genes in congenital long QT syndrome. Human mutation 2002 Nov 20 (5): 382-91. Jongbloed Roselie, Marcelis Carlo, Velter Crool, Doevendans Pieter, Geraedts Joep, Smeets Hube Similar articles in PubMed