In contrast to these results we (data not shown) and others [44], [63] have found that some DSC2-fluorescent protein chimeras carrying other ARVC associated variations (DSC2-p.R203C, -p.I231T, -p.T275M, -p.D350Y, -p.A897KfsX4) were mislocalised as compared to the wild-type protein. This evidence concerns the gene DSC2 and arrhythmogenic right ventricular cardiomyopathy.