Computational Study on Effect of KCNQ1 P535T Mutation in a Cardiac Ventricular Tissue
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cell Biology,Physiology,Biophysics
Link
https://link.springer.com/content/pdf/10.1007/s00232-023-00287-9.pdf
Reference28 articles.
1. Adeniran I, McPate MJ, Witchel HJ et al (2011) Increased vulnerability of human ventricle to re-entrant excitation in hERG-linked variant 1 short QT syndrome. PLoS Comput Biol 7:e1002313. https://doi.org/10.1371/journal.pcbi.1002313
2. Amirian A, Dalili SM, Zafari Z et al (2018) Novel frameshift mutation in the KCNQ1 gene responsible for Jervell and Lange-Nielsen syndrome. Iran J Basic Med Sci 21:108–111. https://doi.org/10.22038/IJBMS.2017.23207.5908
3. Barhanin J, Lesage F, Guillemare E et al (1996) K(V)LQT1 and lsK (minK) proteins associate to form the I(Ks) cardiac potassium current. Nature 384:78–80. https://doi.org/10.1038/384078a0
4. Cooper DN, Stenson PD, Chuzhanova NA (2006) The human gene mutation database (HGMD) and its exploitation in the study of mutational mechanisms. Curr Protoc Bioinforma. https://doi.org/10.1002/0471250953.bi0113s12
5. Gima K, Rudy Y (2002) Ionic current basis of electrocardiographic waveforms: a model study. Circ Res 90:889–896. https://doi.org/10.1161/01.RES.0000016960.61087.86
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