DYSF and neuromuscular disease caused by qualitative or quantitative defects of dysferlin: In this experiment, we utilized the iPSC line CiRA00396 derived from a patient with Miyoshi myopathy (a form of dysferlinopathy), who has a homozygous recessive nonsense mutation of c.C3166T (p.Arg1056Ter) at exon 29 in the Dysferlin (DYSF) gene (Liu et al., 1998).