TRIM32 and myopathy: The mutation c.1459G > A/p.D487N in the TRIM32 gene, identified as a founder mutation in Hutterite population, has been the most frequently reported [15], but a recent series of 12 non-Hutterite patients with a TRIM32-related myopathy, with mutations located both in the NHL and coiled-coil domains, has been described [21].