TRIM54 and congenital myopathy 7A, myosin storage, autosomal dominant: However, double-knockout (MuRF1−/−;MuRF3−/−) mice display a skeletal and cardiac muscle myopathy presenting similarly to human Myosin Storage Myopathies [148], which coupled with similar binding targets, [152] suggests that some functional redundancy exists between MuRF family members.