Further filtering for variants in genes linked with DCM from Human Gene Mutation Database (HGMD) [13] revealed 48 variants, of which two were located in exons: PLN: c.26G > T:(p.Arg9Leu) in phosholamban and DES:c.665G > A:(p.Arg222His) (rs367961979) in desmin. Here, DES is linked to familial dilated cardiomyopathy.