Fig. 1From: Reporting a rare form of myopathy, myopathy with extrapyramidal signs, in an Iranian family using next generation sequencing: a case reporta Pedigree of the family with two affected children (filled symbols). b Sequence chromatograms of c.1294_1295delA mutation in the affected proband V1 are shown in homozygous form (up) compared to heterozygous form (her mother (IV2) (down)). Site of the deletion is shown with arrowsBack to article page