Fig. 4
From: Case report: exome sequencing achieved a definite diagnosis in a Chinese family with muscle atrophy
Sanger sequencing and co-segregate validation of candidate mutations. Sanger sequencing results of (a) the c.218C > G, p.Ser73* mutation of GDAP1; (b) the c.1262C > T, p.Thr421Met mutation of ARHGEF11; (c) the c.2029C > T, p.Arg677Cys mutation of ARHGEF11. ①-⑥ are represented as genotypes of normal control, I-1, I-2, II-1, II-2 and II-3, respectively