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. 2019 May 21;40(37):3081–3094. doi: 10.1093/eurheartj/ehz308

Take home figure.

Take home figure

The p.R211H mutation in the gene encoding RAD GTPase is involved in Brugada syndrome pathogenesis, leading to both electrical and structural defects in cardiomyocytes differentiated from induced pluripotent stem cells of affected patients.