PICILLO, E. .; TORELLA, A.; PASSAMANO, L.; NIGRO, V.; POLITANO, L. Autosomal dominant Ullrich congenital muscular dystrophy due to a de novo mutation in COL6A3 gene. A case report. Acta Myologica, [S. l.], v. 41, n. 2, p. 95–98, 2022. DOI: 10.36185/2532-1900-073. Disponível em: https://www.actamyologica.it/article/view/124. Acesso em: 22 dec. 2024.