Susceptibility to Ventricular Arrhythmias Resulting from Mutations in FKBP1B, PXDNL, and SCN9A Evaluated in hiPSC Cardiomyocytes

Figure 3

Pedigree of the proband (denoted with arrow) and family. Genetic analysis revealed that each parent carried different heterozygous mutation(s). The father (1239) carried the FKBP1b mutation, whereas the mother (1240) carried the PXDNL and SCN9A mutations. The sister of the proband (1241) only inherited the mutation in SCN9A. Both parents and the sister were asymptomatic.