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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 7 (of 7 Records)

Query Trace: Disease and SCN4B[original query]
Mutations in sodium channel ß1- and ß2-subunits associated with atrial fibrillation.
Circulation. Arrhythmia and electrophysiology 2009 Jun 2 (3): 268-75.
Watanabe Hiroshi, Darbar Dawood, Kaiser Daniel W, Jiramongkolchai Kim, Chopra Sameer, Donahue Brian S, Kannankeril Prince J, Roden Dan
Mutations in sodium channel ß-subunit SCN3B are associated with early-onset lone atrial fibrillation.
Cardiovascular research 2011 Mar 89 (4): 786-93.
Olesen Morten S, Jespersen Thomas, Nielsen Jonas B, Liang Bo, Møller Daniel V, Hedley Paula, Christiansen Michael, Varró András, Olesen Søren-Peter, Haunsø Stig, Schmitt Nicole, Svendsen Jesper
Sodium current and potassium transient outward current genes in Brugada syndrome: screening and bioinformatics.
The Canadian journal of cardiology 0 28 (2): 196-200.
Holst Anders G, Saber Siamak, Houshmand Massoud, Zaklyazminskaya Elena V, Wang Yinman, Jensen Henrik Kjærulf, Refsgaard Lena, Haunsø Stig, Svendsen Jesper Hastrup, Olesen Morten S, Tfelt-Hansen Jac
Results of genetic testing in 855 consecutive unrelated patients referred for long QT syndrome in a clinical laboratory.
Genetic testing and molecular biomarkers 2013 Jul 17 (7): 553-61.
Lieve Krystien V, Williams Leah, Daly Amy, Richard Gabriele, Bale Sherri, Macaya Daniela, Chung Wendy
Is sudden unexplained nocturnal death syndrome in Southern China a cardiac sodium channel dysfunction disorder?
Forensic science international 2014 Mar 236 38-45.
Liu Chao, Tester David J, Hou Yiding, Wang Wen, Lv Guoli, Ackerman Michael J, Makielski Jonathan C, Cheng Jiandi
Contribution of Cardiac Sodium Channel ß-Subunit Variants to Brugada Syndrome.
Circulation journal : official journal of the Japanese Circulation Society 2015 Jul .
Peeters Uschi, Scornik Fabiana, Riuró Helena, Pérez Guillermo, Komurcu-Bayrak Evrim, Van Malderen Sophie, Pappaert Gudrun, Tarradas Anna, Pagans Sara, Daneels Dorien, Breckpot Karine, Brugada Pedro, Bonduelle Maryse, Brugada Ramon, Van Dooren Son
Diagnostic yield and variant reassessment in the genes encoding Nav1.5 channel in Russian patients with Brugada syndrome.
Frontiers in pharmacology 2022 9 13 984299.
Zaklyazminskaya Elena, Shestak Anna, Podolyak Dmitry, Komoliatova Vera, Makarov Leonid, Novitskaya Anna, Revishvili Amir
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