Rare diseases affecting muscles are predominantly genetic muscle disorders, such as Duchenne muscular dystrophy, progressive muscular dystrophy, facioscapulohumeral muscular dystrophy, myotonic dystrophy, spinal muscular atrophy, peroneal muscular atrophy, glycogen storage diseases, lipid metabolism myopathies, and mitochondrial encephalomyopathies. Cyagen has developed a series of gene knockout, knock-in, and point mutation models for muscular diseases. We also offer customization and collaboration options to meet the specific needs of researchers.