Generation of gene-corrected human isogenic iPSC lines from hypertrophic cardiomyopathy patients harboring PRKAG2 mutation (c.2084A>G, p.His530Arg) using prime editing
Stem Cell Res. 2026 May 1;94:104008. doi: 10.1016/j.scr.2026.104008. Online ahead of print.ABSTRACTPRKAG2 cardiac syndrome is a rare inherited cardiomyopathy characterized by clinical manifestations such as...
