CROCI, C.; TRAVERSO, M.; BARATTO, S. .; IACOMINO, M. .; PEDEMONTE, M.; CAROLI, F.; SCALA, M.; BRUNO, C.; FIORILLO, C. Congenital myopathy associated with a novel mutation in MEGF10 gene, myofibrillar alteration and progressive course. Acta Myologica, [S. l.], v. 41, n. 3, p. 111–116, 2022. DOI: 10.36185/2532-1900-076. Disponível em: https://www.actamyologica.it/article/view/126. Acesso em: 3 may. 2024.