Fig. 2From: Novel compound heterozygous variants in the RPL3L gene causing dilated cardiomyopathy type-2D: a case report and literature review(A) The distribution of all variants detected so far in eight dilated cardiomyopathy patients with RPL3L variants. (B) Sanger sequencing DNA chromatograms of RPL3L indicating the frameshift c.1074dupA(p.Ala359fs*6) variant inherited from the mother and the missense variant c.80G > A / p.Gly27Asp was a de novo variantBack to article page