Fig. 5From: Familial dilated cardiomyopathy caused by a novel variant in the Lamin A/C gene: a case reportPedigree of the family and chromatograms of the c. 1325 T>C (p. Val442Ala) heterozygous LMNA gene variant. Among other relatives, only the proband’s father’s brother (II-6) received genetic sequence analysis for this LMNA variant, but no variant was foundBack to article page