For example, Olive et al. [106] reported studies in small cohorts of patients with myotilinopathy—a disease that has been associated with variable syndromes including limb girdle muscular dystrophy type 1a and a subgroup of patients with a myofibrillar myopathy due to mutations in the myotilin gene (MYOT). This evidence concerns the gene MYOT and myofibrillar myopathy.