Fig. 8From: Identification of novel pathogenic variants of Calpain-3 gene in limb girdle muscular dystrophy R1Heterozygous missense variant in exon 22 of CAPN3 gene (Patient 3) [NM_000070.3 (CAPN3): c.2338G > C; NP_000061.1: p.Asp780His (rs778768583)] [a - control, b– patient, c- patient’s father]Back to article page