Potassium voltage-gated channel subfamily E regulatory subunit 1
genes
References
Abbott GW. KCNE1 and KCNE3: The yin and yang of voltage-gated K(+) channelregulation. Gene. 2016 Jan 15;576(1 Pt 1):1-13. doi: 10.1016/j.gene.2015.09.059.
Alders M, Bikker H, Christiaans I. Long QT Syndrome. 2003 Feb 20 [updated 2018Feb 8]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K,Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University ofWashington, Seattle; 1993-2020. Available fromhttp://www.ncbi.nlm.nih.gov/books/NBK1129/
Chan PJ, Osteen JD, Xiong D, Bohnen MS, Doshi D, Sampson KJ, Marx SO, KarlinA, Kass RS. Characterization of KCNQ1 atrial fibrillation mutations revealsdistinct dependence on KCNE1. J Gen Physiol. 2012 Feb;139(2):135-44. doi:10.1085/jgp.201110672.
Ehmke H. Physiological functions of the regulatory potassium channel subunitKCNE1. Am J Physiol Regul Integr Comp Physiol. 2002 Mar;282(3):R637-8. Review.
Lundquist AL, Turner CL, Ballester LY, George AL Jr. Expression andtranscriptional control of human KCNE genes. Genomics. 2006 Jan;87(1):119-28.
Melman YF, Um SY, Krumerman A, Kagan A, McDonald TV. KCNE1 binds to the KCNQ1 pore to regulate potassium channel activity. Neuron. 2004 Jun 24;42(6):927-37.
Paulussen AD, Gilissen RA, Armstrong M, Doevendans PA, Verhasselt P, SmeetsHJ, Schulze-Bahr E, Haverkamp W, Breithardt G, Cohen N, Aerssens J. Geneticvariations of KCNQ1, KCNH2, SCN5A, KCNE1, and KCNE2 in drug-induced long QTsyndrome patients. J Mol Med (Berl). 2004 Mar;82(3):182-8.
Tranebjærg L, Samson RA, Green GE. Jervell and Lange-Nielsen Syndrome. 2002Jul 29 [updated 2017 Aug 17]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE,Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2020. Available fromhttp://www.ncbi.nlm.nih.gov/books/NBK1405/
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