IACONO, S.; LUPICA, A.; DI STEFANO, V. .; BORGIONE, E.; BRIGHINA, F. A novel compound heterozygous mutation in PYGM gene associated with McArdle’s disease. Acta Myologica, [S. l.], v. 41, n. 1, 2022. DOI: 10.36185/2532-1900-067. Disponível em: https://www.actamyologica.it/article/view/115. Acesso em: 19 jun. 2024.