PIZZA*, A.; PICILLO*, E.; ONORE, M. E.; SCUTIFERO, M.; PASSAMANO, L.; NIGRO, V.; POLITANO, L. 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, [S. l.], v. 42, n. 1, 2022. DOI: 10.36185/2532-1900-246. Disponível em: https://www.actamyologica.it/article/view/246. Acesso em: 1 mar. 2024.