BELHASSEN, I.; MENASSA, R. .; SAKKA, S.; MICHEL-CALEMARD, L.; STREICHENBERGER, N.; BEN AYED, D.; BOUATTOUR, N.; DAMMAK, M.; MHIRI, C. Mild limb girdle muscular dystrophy R9 phenotype caused by novel compound heterozygous FKRP gene mutation: Novel FKRP gene mutation . Acta Myologica, [S. l.], v. 42, n. 4, p. 106–112, 2023. DOI: 10.36185/2532-1900-391. Disponível em: https://www.actamyologica.it/article/view/391. Acesso em: 1 mar. 2024.