Fig. 3

Electropherogram curves and sequences of (a) the wildtype sequence and (b) the index patient: The index patient shows the frameshift mutation c.1664delT (p.F555Sfs*8) in the PKP2-gene. c Pedigree of the index patient (II.2) displaying an autosomal dominant inheritance pattern. Her father (I.2) is also diagnosed with ARVC and both children (III.1 and III.2) are mutation carriers, the son (III.2) fulfills the 2010 Task Force criteria of ARVC and is diagnosed with the disease