ANO5 and autosomal recessive limb-girdle muscular dystrophy type 2L: Interestingly, genetic defects in ANO5 were also identified to be responsible for two types of autosomal recessive muscular dystrophies—limb girdle muscular dystrophy type 2L (LGMD2L) and Miyoshi myopathy type 3 (MMD3) with characteristics that resemble dysferlinopathies [19–25].