BARP, A.; NERI, L. M.; MAGGI, L.; IASCONE, M.; GUALANDI, F. . A novel deep intronic mutation expands the genotype spectrum of MYH7-related myopathies. Acta Myologica, [S. l.], v. 44, n. 3, 2025. DOI: 10.36185/2532-1900-1282. Disponível em: https://www.actamyologica.it/article/view/1282. Acesso em: 6 oct. 2025.