Skip to main content
. 2018 Jun 1;59(5):698–701. doi: 10.3349/ymj.2018.59.5.698

Fig. 2. Pedigree and electropherogram findings of three limb-girdle muscular dystrophy type 1D patients. (A) Pedigree of patient 1. (B) Electropherogram presents a mutation in DNAJB6 genomic DNA (c.265T>A; p.Phe89Ile). (C) Novel mutation in patient 2 and his father (his mother's sequencing showed no variant in DNAJB6).

Fig. 2