Generation of two iPSC lines from dilated cardiomyopathy patients with pathogenic variants in the SCN5A gene
Author:
Funder
American Heart Association Inc
Publisher
Elsevier BV
Reference5 articles.
1. Patient-specific induced pluripotent stem cell-based disease model for pathogenesis studies and clinical pharmacotherapy;Li;Circ. Arrhythm. Electrophysiol.,2017
2. SCN5A variants: Association with cardiac disorders;Li;Front. Physiol.,2018
3. Generation of two iPSC lines from hypertrophic cardiomyopathy patients carrying MYBPC3 and PRKAG2 variants;Manhas;Stem Cell Res.,2022
4. Cardiomyopathy Registry Research, SCN5A mutations associate with arrhythmic dilated cardiomyopathy and commonly localize to the voltage-sensing mechanism;McNair;J. Am .Coll. Cardiol.,2011
5. Gating pore currents are defects in common with two Nav1.5 mutations in patients with mixed arrhythmias and dilated cardiomyopathy;Moreau;J. Gen. Physiol.,2015
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