ANO5 and autosomal recessive limb-girdle muscular dystrophy type 2L: Previously, ANO5 gene mutations were found to be responsible for autosomal recessive muscular dystrophies, e.g., Limb girdle muscular dystrophy type 2L (LGMD2L, MIM:611307) and Miyoshi-like myopathy (MMD3, MIM:613319).