Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Abnormalities and KCNJ8[original query] |
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Gain-of-function mutation S422L in the KCNJ8-encoded cardiac K(ATP) channel Kir6.1 as a pathogenic substrate for J-wave syndromes. Heart rhythm : the official journal of the Heart Rhythm Society 2010 Oct 7 (10): 1466-71. Medeiros-Domingo Argelia, Tan Bi-Hua, Crotti Lia, Tester David J, Eckhardt Lee, Cuoretti Alessandra, Kroboth Stacie L, Song Chunhua, Zhou Qing, Kopp Doug, Schwartz Peter J, Makielski Jonathan C, Ackerman Michael |
A KCNJ8 mutation associated with early repolarization and atrial fibrillation. Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology 2012 Oct 14 (10): 1428-32. Delaney Jessica T, Muhammad Raafia, Blair Marcia A, Kor Kaylen, Fish Frank A, Roden Dan M, Darbar Dawo |
The KCNJ8-S422L variant previously associated with J-wave syndromes is found at an increased frequency in Ashkenazi Jews. European journal of human genetics : EJHG 2014 Jan 22 (1): 94-8. Veeramah Krishna R, Karafet Tatiana M, Wolf Daniel, Samson Ricardo A, Hammer Michael |
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- Page last updated:Apr 16, 2024
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