Fig. 3From: DMDtoolkit: a tool for visualizing the mutated dystrophin protein and predicting the clinical severity in DMDA pedigree of BMD father and DMD son. The family has inherited a disease-causing mutation, i.e., Exon45-47del, which led to BMD. Individual 13 was the proband, the BMD father. Individual 23 was his DMD son with a novo mutation of exon48-52delBack to article page