SCN5A and cardiomyopathy, familial restrictive, 1: In 8/12 probands (66.7%), we found likely causative variants in known cardiomyopathy genes (TTN, DSP, SCN5A, TNNC1, TPM1, CRYAB, and MYH7), which were confirmed as de novo (six DCM, one HCM, and one RCM case, Table 1, Figure S1).