Mutations in TRIM32 have been associated to Limb-Girdle Muscular Dystrophy 2H (LGMD2H) and Sarcotubular Myopathy, a form of distal myopathy with peculiar features in muscle biopsy, now considered in the spectrum of LGMD2H. This evidence concerns the gene TRIM32 and autosomal recessive limb-girdle muscular dystrophy type 2H.