Pizza*, A., Picillo*, E., Onore, M. E., Scutifero, M., Passamano, L., Nigro, V., & Politano, L. (2022). Xp21 contiguous gene deletion syndrome presenting as Duchenne muscular dystrophy and glycerol kinase deficiency associated with intellectual disability: case report and review literature. Acta Myologica, 42(1). https://doi.org/10.36185/2532-1900-246